Corrigendum Supply Of Neuros in Jaipur - Complete Tender Details

Corrigendum : Supply Of Neurosurgery Implants - Anterior Cervical Plating System Non Variable Angle Screws System. * Profile Of The Plate Must Be 1.8-2mm 2 • 5 * Width Of The Plate Should Be 16-17.5mm * Must Be Commercial Pure Medical Grade Titanium * Must Have Convergence Of 30 Degree * Cranial Screw Angulation Must Be 6 Degree * Screw Must Be Available From 12mm To 18mm Length, Self Tapping And Self Drilling Options * The System Must Have The Option For Fixed And Variable Angle Screw Guide Which May Work As Plate Holder Too. * Locking Mechanism Of The Screw Must Be On Mono Cortical With Locking Head Expansion Screw Mechanism/ One Step Locking With Elgiloy Clip The Plate Must Be Available In Following Sizes, Cervical Plate Level – 1st, Cervical Plate Level – 2nd, Cervical Plate Level – 3rd, Cervical Plate Level – 4th, Variable Angle Screw System * A Single Plate Must Provide The Option Of Rigid, Toggling And Hybrid Construct. * The Cephalad/caudal Angulation Must Be Of Approx. 28 Degree. With 8degree Of. Offset * The Lateral/medial Angulation Range Must Be Of 14 Degree With 7 Degree Of Offset. * Locking Mechanism Of The Screw Must Be One Step Locking With Elgiloy Clip Should Block The Screws From Coming Out. * The Plate Must Be 1.8 -2.5mm In Thickness And 16-17.5 Mm In Width * The Core Diameter Of The Screws Must Be 3mm With Outer Diameter Being 4.0mm And 4.5mm And Self Drilling "* The Plates Must Be Available In Following Sizes: One Level Plates 22.6_34.6 Mm, Two Level Plates 36.6 54.6mm Three Level Plates 53.6_77.6mm And Four Level Plates" The Plate Us Be Available In Folowing Sizes, Cervical Plate Level - 1, Cervical Plate Level - 2, Cervical Plate Level - 3, Cervical Plate Level – 4, Anterior Cervical Interbody Fusion Device With Screw Mechanism * The Implant Should Act As Standalone Interbody Fusion Device For Cervical Spine With The Benefits Of An Interbody Spacer And An Anterior Cervical Spine. * The Implant Must Be A Combination Of Peek/titanium Must Automatically Align When Inserted "* The Implant Must Have Radio Opaque Marker For Posterior And Anterior Visualization During Imaging And Teeth On Superior And Anterior Surface For Initial Stability" * Spacer Component Must Be Made Of Peek/ Titanium "* The Implant Must Have On One Step Locking Screw And Screw Loading Wire Should From A Bone Wedge With 40° + 5° Cranial/caudal Angle With 2.5° Medial And Lateral Angle." * The Screw Must Come With Self-tapping Or Self-drilling And Self-centering Options With Titanium Alloy Material * The Screw Must Come In 3.0mm To 4.5mm Diameter & Must Be Colour Coded By Screw Lengths Varying From 12-20mm. * The Implants Must Come In Parallel Lordotic And Convex Implants Sets With Heights Varying From 5mm To 12mm With An Increment Of Imm Each. * Should Have Option For 2-4 Screws, Cv Junction Fixation System (occiput To C2) * The System Should Be Versatile. * The System Should Have Medial And Lateral Plates Of 50 & 60mm, One & Two Hole * Clamps Which Must Allow The Medial And Lateral Rod Placement, And Should Be Able To Give * The System Must Have Straight And Pre Contoured 3.5mm Rods, * The System Must Have C2 Screw 3.5 Mm With 4mm Rescue Screws. * The System Should Have Blunt 4.5mm Occipital Screws And 5mm Emergency Screws With 4-18mm Lengths All Compatible With * The System Must Have The Templates Of Occipital Plates To Avoid Wrong Plate Selection. * The System Should Have Simple Locking Mechanism Of Set Screws * The System Should Have Tap For Better Screw Purchase And 2mm Torque Limiting Screw Driver For Final Tightening. * Following Component Should Be Available In System, A) Occipital Plate, B) Occipital Clamp Single Hole, C) Occipital Clamp Double Hole, D) Bone Screw, E) Polyaxial Screw With Locking Cap, F) Rod, G) Transverse Connector, H) Tapered Rod, Top Loading Implant System For Posterior Stabilization Of The Cervical Spine. * The System Should Be Top Loading For The Posterior Stabilization Of The Cervical And Upper Thoracic Spine * The System Should Have Cancellous & Cortex Bone Screws. (titanium) * The System Should Have Locking Screws For Angularly Stable Locking And Fixation Of The Rod. (titanium) * The System Must Have Self-tapping Screws. * The System Must Have 3.5mm Titanium Rod. * The System Should Have Oc Fusion Option. * The System Should Offer Hooks. * The System Should Have Cancellous Profile Bone Screws: 3.5mm: 8mm - 50 Mm (2 Mm Increments) 4.0mm : 8mm - 50 Mm (2 Mm Increments) 4.5mm: 8mm - 50 Mm (2 Mm Increments) * The System Should Have Cortical Profile Bone Screws: 3.5mm : 28 Mm - 50mm (2 Mm Increments) * The System Should Have Screw Head Profile: Height = 1 Mm And Reduction Screw 22mm Height * The System Should Have Rod Run = 9mm * The System Should Have Shaft Screws (cortical Profile):3.5 Mm: 22mm - 36mm (2 Mm Increments) *shaft Screws Should Have 10mm Unthreaded Portion *rods Must Be Of The Following Specifications: 3.5mm Ti Rod: 80 Mm, 120 Mm And 240 Mm Lengths 3.5mm /5.0mm Ti Rod, 120 Mm /170 Mm 3.5mm /6.0mm Ti Rod, 120 Mm /170 Mm * The System Should Have Transconnector: 60mm And 75mm * The System Should Have Short And Long/left And Right Hooks * The System Should Have 3.5mm Ti Transverse Bar * The System Should Have Occipital Plate/rods Options. System Should Have Following Components, A) Polyaxial Screw With Locking Cap, B) Rod, C) Transverse Connector, D) Cervical Hook, Disc Prosthesis For Cervical Spine * Superior And Inferior Implant Plate Made Of Cobalt - Chromium - Molybdenum/titanium Alloy According Iso 5832-12 * Plasma - Sprayed Titanium Coating, Ti According Iso S832- 2 * Inlay Made Of Ultra - High Molecular Weight Polyethylene (uhmwpe) * Ball And Socket Principle_ Metal On Polymer/metal. * Modular Anatomical Design -optimal Primary Stability Due To H Keel Anchorage Of The Prosthesis In The Vertebral Body. -anatomical Footprint Design For Maximum Endplate Coverage * Six Different Footprints Available For Optimal Coverage Of The Vertebral End Plate: M, Md, L, Ld, Xl, Xld * Three Different Heights (5,6, And 7mm) Allowing Adjustment To The Individual Dimensions Of The Patients Disc., Anterior Cervical Interbody Fusion Device. * The Implant Should Act As Standalone Interbody Fusion Device For Cervical Spine With The Benefits Of An Interbody Spacer And An Anterior Cervical Plate. * The Implant Must Be A Combination Of Plate And Spacer Wherein The Plate Must Automatically Align When Inserted. * The Implant Must Have Radio Opaque Marker For Posterior Visualization During Imaging Teeth On Superior And Anterior Surface For Initial Stability. * Spacer Component Must Be Made Of Peek Optima (polyetheretherketone) * The Implant Must Have One Step Locking Screw And Screws Should Form A Bone Wedge With 40*- 5 Cranial/caudal Angle With 2.5 Degree Medial Lateral Angle. * The Screw Must Come With Self-tapping And Self-centering/drilling Option, With Titanium Alloy Material (ti-6ai-7nb) * The Screws Must Come In 3.0mm To 4.5mm Diameter & Must Be Colour Coded By Screw Length Varying From 12mm To 18mm. * Implants Triobular Thread Cutting Flutes Should Be Self Centering. *the Implants Must Come In Parallel Lordotic And Convex Implant Sets With Heights Varying From 5mm To 12mm With An Increment Of 1mm Each., Expandable Corpectomy Cages. * Expandable Vertebral Body Replacements. * For Cervical & Upper Thoracic Spine. * Should Have Ratchet System So That Desired Height Can Be Achieved. * Should Achieve Height From 17mm To 70mm & Angle From 4.5 To 7 Degree, Expandable Titanium Cage With Footprint * Should Be Made Up Of Medical Approved Good Quality Titanium. * Foot Print Size - 12x/4mm,21x23mm, 25x 32mm * Expanding Height Range From 15-89 Mm For Cervical 24-70 Mm F O R Thoracic 29- 119 For Lumber * One Instrument To Insert And Expand The Implant * It Should Have Smooth In Situ Continuous Expansion * Captured Locking Screw * Multiple Insertion Angles To Accommodate Various Approaches * Should Have Window For Post Insertion Bone Graft Packing * Large Open Canal For Bone Graft Material, Titanium Mesh Cage For Vertebral Body Replacement Per Mm.10-12-15mm Diameter, A) For Cervical Round / Oval, B) Thoraco / Lumber-round /oval, Sublaminar Titanium Cable System * The Cable Should Be Made Of Multiple Strands Of Titanium To Enable Better Grip Over Tissues. It Should Be Available 1mm Diameter, Lengh Should Be 18.25-22 Inch . * The Individual Packaging Should Be Available In Double Cable And Single Cable Individual Sterilized Packaging. * It Should Be Malleable With Crimp. * It Should Withstand Twisting And Knotting Without Loosing Its Tensile Strength. * It Should Have A Built In Crimp To Enable Fixation Without Having To Tie A Knot And Have Optimal Tension After Fixation. * I T Should Be Of Medical Grade Titanium And Should Be Artefact Free On Mri And Ct., A) Titanium Double Cable With Integral Crimp - 10 Nos., B) Titanium Single Cable With Integral Crimp - 25 Nos., Cage And Titanium Staples For Anterior Fixation * Titanium Mesh Cage System For Management Of Cervical & Thoraco-lumbar Burst Fractures And Tumors That Permits Anterior Load Sharing, Allows For Distraction To Perform Reduction And Compression Of The Bone Graft. * Should Have Anterior Staples For 13/15 * Should Have Titanium Mesh Cages For The Cervical, Thoracic, Lumbar And Interbody Fusion. * Cervical Cages 10 X 70mm, 13x70mm, 10x100mm - 15 Each * Thoracic Cages 13x30mm, 16x30mm, 16x60mm - 15 Each * Lumbar Cages 19x40mm, 19x 90mm, 13x10mm - 15 Each * Kidney/bullet Shaped Cages For Tlif - 15 Each * Anterior Staples For 13 & 15mm - 15 Each Anterior Double Rod Staples 21,23,25mm -should Have, A) Single Hole Staples, B) Double Hole Staples, Poly Ether-ether Ketone (peek) Spacer For Cervical Spine * Spacer Shouid Be Made Of Radiolucent Poly Ether - Ether Ketone. * Should Be Designed For Use With Open, Mini And Endoscopic Technique. * Should Have Space For Filling The Bone Graft. * Should Be Of Anatomical Design To Fit The Cervical Spine. * Should Be Available In Various Sizes. * Should Have Radio Opaque Marker To Identify The Location Of The Spacer At The Time Of Placement, Odontoid Screw * Screw Should Made Up Of Tianium Alloy (tan). * Screw Should Be Cannulated * Screw Should Be Self-drilling. * Screw Should Consist Of 12mm Short Thread * Screw Should Be Of 3.5mm Diameter. * Screw Should Be Available In The Length Of 36mm To 50mm. The Whole System Should Thus Enable The Following. Help In Preservation Of Alantoaxial Mobility With Lag Screw Compression Technique. With Wire Guiding Ensures Precise Positioning Of Implants & Instruments., C1 - C2 Transarticular Screw * Screw Should Made Up Of Titanium Alloy (tan) * Screw Should Be Self-tapping Cortex Screw. * Screw Should Be Of 3.5mm Diameter. * Screw Should Be Available In The Length Of 30mm To 60mm. * Screw Should Consist Of Threaded Socket In Screw Head, C1 -c2 Spacer * Joint Spacer Size 3.5 Mm, 4.5mm, 5mm, 6mm * Joint Spacer Made Up Of Titanium * Should Be Tapered In The Front And There Should Be Able To Attach To The Instrument For Insertion, Side Opening Pedicle Screw System * The System Must Have Side Opning Pedicle Screws And Hooks For Posterior Fixation Of Spine. * The System Should Be Compatible With Shantz Screw, Hooks, Clamps, Side Opening Pedicle Screw And Variable Axis Screw * The Side Loading Pedicle Screw Should Be Available In 5,6 & 7mm Diameter With Varying Length Available In 30mm To 60mm With 5mm Increment. * The System Must Have Side Opening Right & Left Lamina And Pedicle Hooks., Top Loading Pedicle Screw System * Top Loading Preassembled Polyaxial Pedicle Screw With Dual Core, Titanium Alloy Tan (ti A16 N7) With Following Specification And Colour Coding: Diameter 4mm To 8mm, Lengths 20mm To 100mm * Angulations Of The Screw Head Of 25 To 50 Degree In All Direction. * 3.5mm Hexagonal Locking Cap Based On Titanium Break Off Plug Locking Mechanism. * Two Step Locking Mechanism With Initial Locking With Locking Cap And Final Locking With Blue Set Screw * The Option Of Achieving Case Specific Lordotic And Parallel Compression With The Same System. * Curved Rods In 6mm Diameter From 45mm To 85mm In The Increments Of 5mm Straight Rod In 6mm Diameter From 50mm To 150mm System Shouid Have Following Parts., A) Polyaxial Screw, B) Monoaxial Screw, C) Hook, D) Rod, E) Transvers Connector, F) Reduction Screw, Transformaminal Lumbar Interbody Fusion. (tlif) * The Cage Must Be Radiolucent Made Up Of Peek - Optima Material With Sharp Teeth Designed For Transformational Lumbar Interbody Fusion (tlif) * The Cages Must Have Rounded Tapering Edges/kidney Shape Allowing Easy Insertion Thus Minimizing Injuries To Endplates And Neural Structures. * The Cage Should Be Able To Move Upto 80 Degree After Attaching With One Key Instrument. * The Cage Must Have 3 Titanium Markers (two Lateral, One Central) To Indicate The Cage Position On X Ray. * The Cages Must Have Injection Moulded Roughened Surface Promoting Bone Integration And Ongrowth. * The Cages Must Have Biconvex Shape Providing Even Distribution Of Compressive Forces Along The Endplates Thus Stability. * The Cages Must Have One Broad Graft Hole And Two Lateral Holes. * The Cages Must Be Pre Filled With Chromos, Synthetic Bone Graft. * Implants Must Be Available In Two Footprint Sizes 10x27mm And Are Available As Sterile Packed. * The Available Implant Heights Must Be 7mm,8mm, 9mm, 10mm, 11mm, 12mm, 13mm, 15mm, 17mm,, Posterior Lumber Interbody Fusion Plif. * The System Should Be Able To Provide: Adequate Stability Restores Disc Height Restores Lordosis Preserves The Integrity Of The Vertebral Body Endplates Provides An Optimized Fusion Bed. * Interbody Fusion Cage System Of Implants And Instruments For Posterior Lumbar Interbody Fusion (plif) * Cage Must Be Made Of Peek Material Preferably Radiolucent. * Cage Must Have Two X-ray Markers Integrated Into The Cages To Enable Easy Visualization Of Their Position Postoperatively. * Peek Material Used Must Contain No Carbon Fibers, Thereby Reducing The Risk Of Systemic Uptake And Local Inflammatory Response. * Cages Must Be Available In 6 Heights In 2mm Increments, And Should Be Supplied Sterile Pre-packed. * The Optimal Anatomical Shape And Supportive Superior And Inferior Surface Design Of The Cage Should Reduces The Risk Of Subsidence Into The Adjacent Vertebrae. * The Cage Should Have Perforated Structure Which Must Allows For Bony Ingrowth Through The Cage, And The Design Must Ensures Optimal Implant-to-endplate Contact * Cage Must Be Designed For An Optimal Fit Into The Natural Concavity Between T W O Adjacent Vertebral Bodies. * Cage Must Have Teeth On The Superior And Inferior Surfaces Providing Additional Primary Stability. * The Cage Must Be Injection Moulded Peek Cage So That It Has Roughened Surface, Which Is Superior To A Machined Peek Surface In That It Promotes Bone Integration And Ongrowth., Anterior Stabilization Of Thoraco-lumbar Spine * The Implant Should Provide Anterior Stabilization To Thoracolumber Spine. * The Implant Should Provide The Benefit Of Palte And Rod Construct And Be Designed To Be Used Along With Either Bone Graft Or With A Vertebral Body Replacement. * The Implant Should Come With Instruments Which Are Designed For Use In Open, Minimal-open Or Endoscopically Assisted Approaches. * The Implant Should Come With Telescopic Mechanism With The Facility Of In Situ Compression And Distraction. * The Implants Should Come In The Following Sizes: Mono-segmental: 29-33mm, 31-37mm, 35-45mm, 41-57mm, Bi-segmental: 53-71 Mm, 66-86mm * Height Of The Implant Above Bone Without Posterior Locking Screws Should Be 7.7mm And With Posterior Locking Screws Should Be 9.0mm And Convergence Of Screws Should Be Of 7.0 * The Posterior Screws Should Be Of 7.0mm Diameter, Cannulated For Use With K-wire, Dual Core And Double Lead. * The Implants Should Come With Polyaxial Bushings Which Allow An Angulations Of +15 For Screw Insertion Tailored To The Individual Anatomical Situation., Artificial Lumbar Disc * Should Be Two Piece Design Metal On Metal Construct With Both Options For True Anteriorand Oblique Insertion. * Should Be Made Available In All The 3 Sizes Small, Medium And Large And 10,12,14mm In Height. * Should Have Butterfly Shaped Device For Intervertebral Assisted With Motion With Silicon Bumper In Polyester Jacket 8mm. 10mm. 12mm. 14mm, Kyphoplasty And Vertebroplasty Kit * The Kit Should Be Pre-sterile. * Should Have Working Cannulas With Inner Diameter 3.2mm Or Less Outer Diameter 4.2mm Or More With Calibration Along With Cannulated Obturator. * Should Have Calibrated Drill With Cm/mm Marking On Proximal End. * Should Have Digital Battery Operated Inflation Syringe To Inflate Balloon Showing Pressure In Psi & Atm, Inflation Time And Volume Of Cavity Created In Vertebral Body. * The Inflatable Balloon Tamps Size - 10/3,15/3,20/, (either Size) Should Be Capable To Bear Pressure Of 400 Psi Or More To Elevate Vertebral Body. * The Bone Filling Device Should Be Calibrated And Should Contain Minimum 1.5cc Of Volume. * Should Have Curette For Scrapping Bone In Old V C With Variable Angles 30,60,90 Degree To Create Cavity In Vertebral Body. * The Biopsy Needle Should Have Cm Marking On Proximal Side To Take Adequate Bone Biopsy. * Minimally Invasive, Percutaneous, Balloon Kyphoplasty System For Stabilizing Vcfs * Anerior Radio-opaque Marker On Balloon Tamp Should Mark The Anterior Edge Of The Balloon. * System Components Should Be Available Individually As Well As In Kit Form Including The Following Instruments. * Should Be Supplied With Green High Viscosity Vtp Cement. * Kit Should Have The Following: * 2 Units Of 11 Gauge Bone Access Needle * 1 Introducer Kit Including * Introducer With Extra Cannula * Drill With Drill Tip * At Least 4 Guide Pins * 2 Balloon Tamps * 2 Digital Balloon Inflators * 6 Bone Filler, A) Kyphoplasty Set, B) Vertebroplasty Set, Multilevel Percutaneous Pedicle Screw Fixation For Thoraco Lumbo - Sacral Fixation. * The System Should Be Available For Demonstration As Per The Requirement Of User Department. * The Firms Quoting Should Supply All Above Items * Minimally Invasive Multilevel Percutaneous Pedicle Screw Fixation System For Thoracic As Well Lumbar Fixation With Capability Of Putting At Least 8 Screws Percutaneously. * Compatible With Separate Incision Technique For Screws And Rods. * The System Should Have Capability Of Trauma, Degenerative And Deformity Correction Percutaneously. * System Should Have Straight Rod And It Should Have Straight And Prebended (lordosed And Kyphosed) As Per The Anatomy Of Thoracic And Lumber. * System Should Have The User Friendly Instruments. Sysem Should Have Steerable Rod Inserter And Reduction Screw Extenders. * The Reduction Screw Extender Should Have Large Window At The Base Of The Screw Extenders. * Extenders Should Have Capability Of Step Wise Reducing The Rod On To The Saddle Of The Screw * System Should Have Cannulated Instruments For Ease Of Working On Guide Wires * Screw Sleeves Should Have Specific Markers Which Enable Surgeons To Understand The Reduction Capabilities. * System Should Have Free Hand Rod Inserter Instrument. * System Should Have For Measuring And Rod Confirmation Tool Which Help Surgeon To Check The Insertion Of The Rods On To The Screws Percutaneously. * System Should Provide Unique Method Of Compression And Distraction, Rod Approximation And Rod Rotation (through The Percutaneous Route) * System Should Allow Gradual Dilation To Minimize Muscle Trauma, Fascia Disruption And Blood Loss. * System Should Be Compatible With Both Mono And Multi Axial Screws Capabilities. * The Screws Should Have Reverse Threaded Technology To Reduce Pullout Strength * The Implant Should Have Top Loading, Top Tightening And Most Importantly Reverse Thread Technology With Breakoff Plugs. * System Should Have Cannulated Mono And Multi-axial Screws With Angulation Of 28 Degree And Should Be Available In Self Tapping Screws 4.5,5.5,6.5,7.5mm Diameter And Length 25mm -60mm At The Increment Of 5mm * Should Be Compatible For Use With Fenestrated Screws For Augmenting Vertebral Bodies With Cement. * System Should Be Compatible With 5.5mm Rod * System Should Work With Jamshedi Needle. System Should Have Following Component, A) Pedicle Screw, B) Rod, Hydroxyapetite (ha) Coated Pedicle Screws * Hydroxyapetite Coated Open Ended Reverse Thread Top Loading Top Tighening Fixed Angle Pedicular Screws (assorted Size) 4.5mm, 5.5mm, 6.5mm With Length 30mm-50mm At The Increment Of 5mm With Break Off Type Of Plug With G4 Reverse Thread Technology * Hydroxyapetite Coated Open Ended Reverse Thread Top Loading Top Tightening Multi-axial Pedicular Screws (assorted Size) 4.5mm, 5.5mm, 6.5mm And Should Be Available In Length 30mm-50mm At Increment Of 5mm. * Compatible With Vetebreal Coloum Manipulation And Vertebral Body Rotation Instruments For Deformity Correction. * Universal System Can Be Use Anterior As Well As Posterior Tl Spine * Should Ideally Be Use For Osteoporotic Vertebra/bore * Osteofill Surface Area Of The Screws Threads Should Be Coated With Hydroxyapetite Material. * Should Be Available In Pre-sterile Packs. * All The Implants Must Be Registered With Dgci. System Should Be Available In Following Component, A) Pedicle Screw, B) Rod, C) Transverse Connector, Laminar Hook With Rood - Should Be Made Up To Titanium / Mri Compatible Material And Of Different Size And Angles With Two Rods And Screw. * System Should Be Available In Following Component, A) Pedicle Screw, B) Rod, C) Transverse Connector, Mini Plates & Screws * A Plating System To Offer Neurosurgeons A Choice Do Rigid Fixations Of Craniotomies And Other Cranial Procedures Which Should Be Very Low Profile In Nature And Be A Complete System For A Broad Spectrum Of Cranial Indications Having Following Specifications Technically - * A Modular System Having Autoclave Able Module For Instruments And Implants * Al Plates Are Should Be 0.5mm Thick And Implants Should Be Offered In Various Shapes For An Optimal And Appropriate Choice In The Procedure These Should Include Basic Plates, Frame Plates, Adaption Plates-available In Multi Holes, Burr Hole Covers, Burr Hole Covers For Shunt And Mesh Plates In Various Dimensions (both 0.4mm & 0.6mm Should Be Available) * Temporal & Mastoid Region Should Have Dedicated Plates For Use * Screw Plate Profile Should Be Not More Than 0.6mm For Minimum Palpability * Despite The Minimum Profile, The Plate Strength Should Be Comparable To Thicker Cranial Plates * The Screws Should Be Designed For Hard Cranial Bones And Should Have A Plus Drive Recss For Excellent Screw Retention In The Shaft * The Screws Should Have A Flat Head And Should Be Easy To Pick Up With A Self Holding * The Screws Should Have A Selection In Self-drilling And Self-tapping Types * Screw Lengths Should Be Available In 3-6mm * Emergency Screws Having Different Color Than Regular Screws * The Screwdriver Handle With Hexagonal Coupling Long (66mm) And Short (42mm) Shafts Which Should Be Self Holding In Nature And Compatible With All Screws In The System And Also Fit The Handle Instantly * Holding Instrument For Plates Must Be A Part Of The Instrumentation * A Special Cutter For Strut & Mesh Plates To Be Provided In The System * Appropriate 1.3mm Drill Bits Of 4mm & 6mm Depth Having Stops Appropriate Label Clips For The Screws Which Should Be Replaceable., Plates For Cranial Fixations. * A Clamps System For Rigid Fixation Of Craniotomies * Should Be Easy And Quick Handling As Well As Very Low Profile In Nature * Should Consist Of A Lower And An Upper Plate. The Upper Plate Should Have Optimal, Preferably, A Clover Leaf Design And Shall Be Moveable Upwards And Downwards Along A Central Tube. * The Lower Plate Should Rigidly Fix To The Lower End Of The Tube. * The Clamps Should Be Offered In Diameters Of 13mm To 22mm Enabling Putting Of The Desired Craniotomy Gap, Covering Burr-holes And For Large Gaps Between The Flap And The Skull And Also For Very Large Burr Holes. * The Clamps Should Be Made Of Pure Titanium Which Does Not Provide Any Risks Ot Patients Undergoing Mr Imaging Procedures With Mr Systems Of 1.5 T Or Less. * There Should Be No Magnetic Field Attraction, Heating Is Minor, And Artifacts Involve A Relatively Small Signal Void Comparable To That Of Titanium Plates, Cranial Fixation System * Designed To Assure The Structural Stability Of The Replaced Skull Flap Following A Required Craniotomy Procedure. * Should Have Screw Less Fixation System * Should Have Good Closure Strength * Should Be Radiolucent - Permanent Locks Should Provide Ct And Mr Compatibility, Resulting In Enhanced Image Clarity * Adaptable - Should Have Polymer Material And Design Combine To Augment Ability Of Locks To Contour To The Anatomy * Fast - Should Have Four Simple Steps Require To Fixate A Cranial Flap * Easy To Use - Should Have Intuitive Ergonomic Instrumentation Facilities Handling, External Drainage And Monitoring Used To Manage Csf Drainage * Should Have Tapered Drip Chamber Bottom For Accurately Measuring Small Fluid Volumes * Drip Chambr Should Have 75ml Capacity Should Have Magnifying Lens At Front Of Chamber To Visualize Csf Drip Pulsation * Should Have Hydrophobic Microbial Air Vent Helps Prevent Clogging * Should Have Large Easy To Read Number * Pressure Indicator Window Should Be Easy To Identify * Should Have Colour Stripped Tubing For Easy Identification Of Patient Line * Optional Laser Level For Impoved Accuracy * One System For Both Ventricular And Lumbar Drainage * Should Have Rotating Pressure Scale With Only One Scale Visible At A Time * Mri Safe To 3-tesla (without Laser) * Completely Disposable * Should Have Designated Port For An External Pressure Transducer * Hangs From Iv Pole With Cord Or Attached With Integrate Pole Clamp Should Have Minimum 3 Needle-less Injection Sites For Sampling Cs, Fixed Pressure Ventricedo Peritoneal Of Atrial Shunts With Or W/o Siphon Control Device * Valves Should Be Available In Seven Different Configurations, Including Two With The Siphon Control Device * Should Be Available In Three Shapes, Burr Hole, Contoured And Ultra Small, To Accommodate Different Patient Groups And Different Surgical Preferences * Should Have Three Pressure High, Medium And Low Pressure Paediatric And Adult. * Siphon Control Device Should Allow The Patient To Maintain Icp Within A Normal Physiological Range Regardless Of Flow Rate Or Patient Posture * Pressure Level And Flow Direction Markings Viewable On X-ray * Fixed Pressure Kit Should Include : A One Way Valve, Ventricular Catheter And A Peritoneal Catheter * Should Have Valve Mechanism Fabricated From Dissimilar Materials, Reducing The Possibility Of Valve Sticking * Silicone Reservoir Dome Allows For Injection And Csf Sampling * Polypropylene Needle Guard Should Minimizes The Potential Of A Needle Completely Penetrating The Valve * Should Have Non Metallic Design For Not Interfere With Ct Scans Or Mri * Catheters Should Be Fabricated From Barium-impregnated Tubing With Tantalum Tip To Allow For X-ray Visualization * Length Markers Show Depth Of Penetration During Insertion * Should Have Right Angle Clip Which Provides Non-kinking Bend In The Ventricular Catheter At The Burr Hole Site, Adjustable Pressure Valves/shunts ( Programmable Shunt ) * Should Able To Do Non Invasive Adjustment And Also Should Not Require X-ray Confirmation * Should Be Latex Free * Should Be Mri Compatible * Should Have Valve System With Minimum 10 (ten) Settings. * Should Have Injectable Reservoir Dome * Should Have Distal And Proximal Occluders For Selective Flushing * Should Be Available With And W/o Siphon Control Device (non Siphon Control) * Should Have Portable Handheld Adjustment System And Do Not Require An Outside Power Source * Built In Adjustment Magnet And Lcd Read Out Screen In The Handheld System * Confirmation From X-ray Should Be Optional Not Mandatory * Should Provide Numeric Interpretation (mm H2o) Of The Valve Performance Setting With Included Smart Card * Should Be Powered By Tow Aa Batteries * Programmable Non Siphon Control Lumboperitoneal Shunt Kit Should Also Be Available * Nsc Lp Valve Should Include Integral Lumbar Connector And Strain Relief For Easy, Non Kinking Attachment Of The Proximal Lumber Catheter. * Should Have Small Inner Lumen In Peritoneal Catheter In Nsc Lp Shunt Kit To Preserve Distal Shunt Resistance * Company Main With Magnetic Control Should Available In Jaipur., Titanium Mesh For Cranioplasty * Should Be Made Up Of Titanium And Of Different Sizes. * Should Be Shapable With Screw, Dural Graft Implant (absorbable Collagen Matrix) * Size 1x1" * Should Be Onlay Dural Graft, * Should Be Bioabsorbable, * Suturing / Gluing Should Not Be Required, * Should Be Sterile., Dural Graft Implant (absorbable Collagen Matrix) * Size F1x3"* Should Be Bioabsorbable, * Suturing / Gluing Should Not Be Required, * Should Be Sterile. * Should Be Onlay Dural Graft,, Dural Graft Implant (absorbable Collagen Matrix) * Size 2x2" * Should Be Onlay Dural Graft, * Should Be Bioabsorbable, * Suturing / Gluing Should Not Be Required, * Should Be Sterile., Dural Graft Implant (absorbable Collagen Matrix) * Size 3x3" * Should Be Onlay Dural Graft, * Should Be Bioabsorbable, * Suturing / Gluing Should Not Be Required, * Should Be Sterile., Dural Graft Implant (absorbable Collagen Matrix) * Size 4 × 5 " * Should Be Onlay Dural Graft, * Should Be Bioabsorbable, * Suturing Gluing Should Not Be Required, * Should Be Sterile., Biological Fibrin Glue With Calcium Chloride Human Protein Kit 2 Ml/4ml, Methy Metha Acrylate Bone Cement., Absorbable Porcine Gelatin Based Topical Absorbable Flowable Hemostat With 6cc Syringe Prefilled With Hemostatic Matrix. 2000iu Of Sterile Lyophilized Human Thrombin Total Volume 8 Ml With 14.3 Cm White Applicator Tip And 14.6 Cm Blue Flexible Applicator Tip. Usfda Approved, Absorbable Gelatin Based Topical Flowable Haemostate With Prefilled Syringe., Lumbo Peritoneal Shunt - Designed For Shunting Of Csf From Subarchnoid Space To Peritoneal Cavity - And Should Be Made Up Of Silicon Rubber., Aneurysm Clip (sugita Type) - Should Be Made Up Of Titanium/mri Compatible Material., 1) Straight (s) 7mm, 2 ) Straight (l) 10mm, 3) Bayonet 7mm, 4) Bayonet 10mm, 5) Bent 8mm, 6 ) Slightly Bent, 7) Side Wood Bent 8mm, 8) Side Wood Curved 9mm, 9) Straight Mini Type (s) 4mm, 10) Straight Minitype (l), 11) Bent Minitype 5mm, 12) Bayonet Minitype 5mm, 13) Straight (s) 12mm, 14) Bayonet (s), 15) L Shaped (m) 7.5mm, 16) 45 Angled (l), 17) Straight (m) Fenestrated Large Type 9mm, 18) Bent (m) Fenestrated Large Type 7.5mm, 19) Fenestrated Type Bent (m) 7.5mm, 20) Fenestrated Large Type L-shaped (m) 7.5mm, Disposable Perforator * Should Be Of 9mm, 11mm, 14mm Size. * Should Include Both Burr And Perforator With Dural Guard. * Should Have Colour Code For Size Variation. * Should Be Sterile, Oxidized Regenerated Cellulose Based Topical Absorbable Haemostatic Size 2 × 3", Oxidized Regenerated Cellulose Based Topical Absorbable Haemostatic Size 4 X8"., Oxidized Regenerated Cellulose Based Topical Absorbable Haemostatic Size 2 × 14"., Powdered Exidized Regenerated Cellulose With Prefilled Easy To Use Applicator., Powdered Oxidized Regenerated Cellulose With Endoscope Application., Oblique Lumber Interbody Fusion Device Or Cage- The Implant Must Be Radiolucent Poly Ether Ether Ketone. Should Have Space For Filling The Bone Graft. Should Be Self Distracting Bullet Shaped With Convex Shap Designed To Fit Patient Anatomy. Should Be Available In Various Lordotic Options Of 0 Degree, 6 Degree & 12 Degree & Diameter Start From 8mm To 16mm In Increment Of 2mm. Should Have 5mm Cage Length In Front Of The Cage Markers Which Should Be Visible In Ap Xray View. Should Be Available In Different Lengths 40mm, 45mm, 50mm, 55mm & 60mm. Should Have An Anterior Nose Head Of 5mm For Easier Insertion. Should Be An Impacted Cage System Compatible With Minimally Access Technique. Should Be Able To Undergo Orthogonal Maneuvers., Pedicle Screw System With Cobalt Chrome Multiaxial Head -system Should Have Osteogrip Dual Lead Thread Pattern With A Tapered Tip For Enhanced Fixation At The Bone Implant Interface, Better Closure Mechanism. -system Implant Should Be Equipped With Implant Tracking System Technology & Provide Device Quality And Utilization Related Data. As Per Department Requirement -factory Calibrated Navigated Top Loading Scree With Cobalt Chrome Tulip Head For Strong Fixation & Low Profile To Treat Trauma, Tumor & Degenerative Pathologies. -system Should Be Able To Accommodate Multiple Rod Material Option. - System Should Be Compatible With Enabling Technology Which Is Installed In Organisation. -system Should Be Compatible With 4.5mm To 5.5mm Rod. -system Should Have Option For Titanium Monoaxial Screw & Hooks To Be Used 4.5mm & 5.5mm Rod. -system Should Have Colour Coding For Easy To Use. -system Should Have Ergonomically Designed Instruments., Percutaneous Pedicle Screw Fixation System With Dual Thread Technology- The System Should Single & Multiple Level Capability. The System Should Have Polyaxial/ Monoaxial Screw With Top Loading Locking Mechanism. Implants Should Be Cannulated Poly Axial With 4.5, 5.5 & 6.5mm Dia Screw For Percutaneous Thoraculumber Fixation With Break Off Set Screw. System Should Have Rod Option For Precut & Prebend & Straight Of Different Sizes. System Should Have Free Hand Rod Inserter Instruments. System Should Have For Measuring & Rod Confirmation Tool Which Help To Surgeon To Check The Insertion Of The Rod On To The Screw Percutaneously. System Should Provide Unique Method Of Compression & Distraction. - System Should Be Compatible With Enabling Technology Which Is Installed In Organisation. - System Should Have Cannulated Instruments For Ease Of Working On Guide Wire. The System Should Have Reverse Threaded Technology To Reduce Pullout Strength. Implants Should Be Top Loading, Top Tightening & Most Importantly Reverse Thread Technology. System Should Compatible With 5.5mm Dia Rod. System Should Be Available For Demonstration As Per The Requirement. Implant Head Should Be Made Of Cobalt Chromium Material, Fenestrated Percutaneous Pedicle Screw Fixation System - The System Should Single & Multiple Level Capability. The System Should Have Polyaxial/ Monoaxial Screw With Top Loading Locking Mechanism. Implants Should Be Cannulated Poly Axial With 4.5, 5.5 & 6.5mm Dia Screw For Percutaneous Thoraculumber Fixation With Break Off Set Screw. System Should Have Rod Option For Precut & Prebend & Straight Of Different Sizes. System Should Have Free Hand Rod Inserter Instruments. System Should Have For Measuring & Rod Confirmation Tool Which Help To Surgeon To Check The Insertion Of The Rod On To The Screw Percutaneously. System Should Provide Unique Method Of Compression & Distraction. - System Should Be Compatible With Enabling Technology Which Is Installed In Organisation. - System Should Have Cannulated Instruments For Ease Of Working On Guide Wire. The System Should Have Reverse Threaded Technology To Reduce Pullout Strength. Implants Should Be Top Loading, Top Tightening & Most Importantly Reverse Thread Technology. System Should Compatible With 5.5mm Dia Rod. System Should Be Available For Demonstration As Per The Requirement. Implant Head Should Be Made Of Cobalt Chromium Material System Should Have Option For Cement Insertion System, Demineralized Bone Metrix Bone Substitute- Should Be Having The Capability For Both Osteoconduction And Osteoindution. Should Be Available In Putty Form. Should Be Available In 3 Sizes Based On Volume Of Graft- 1cc, 2.5cc & 5cc. Should Be Available In Sterile Packing., Bmp Graft Single Peotein- Bone Morphogenic Protein (rhbmp2) Size Available In - X Small (1.4cc), Small (2.8cc), Medium (5.6cc), Large (8cc)., Synthetic Bone Graft- Synthetic Bone Grafton Substitute With Recordable Ceramic Granules. -graft Should Have Hydroxyapatite (ha) 15%. -graft Available In Sterile Packaging. -graft Available In Based On Volume 5cc, 10cc, & 15cc., Bone Cement Synthetic Pmma & Hydroxyapatite Combine With Osteoconductivity. -should Be 50% Hydroxyapatite In The Powder Component. -should Be Long Working Time & Low Exothermicity. -should Be In Sterile Packing., Recharge Free Implantable Sacral Neuro Stimulator (mri Compatible): Single - Channel Implantable Sacral Neurostimulator For Use With Mri Compatible Tined Leads, And Patient Programmer, Full Body Mri Compatible & Should Be Compatible With Constant Current. Advanced Programming Features For Patients And Clinicians. • Full Body Mri Compatible With 1.5t And 3t Machines • 7 Distinct Programs With 4 Custom Options • Smart Patient Hand Held Programmer • Mri Mode Should Be Available On The Programmer • Electrode Configuration 4 Lead Electrodes As Anode (+), Cathode (-), Or Off. 1 Case Electrode As Anode (+) Or Off • Amplitude 0 To 12.5 Ma (0.1 Ma Increment) • Rate Rate Range: 3 To 130 Hz • Pulse Width 40 To 450 μs (10 μs Increment) • Cycling Off, On: 2 S To 24 Hrs Softstart/stop Off, On: 1, 2, 4, 8, 15, Or 30 Second Ramp Duration Physical Characteristics Of The Neurostimulator Should Be Maximum Of, • Height 44 Mm (1.7 In) • Length 51 Mm (2 In) • Thickness 7.7 Mm (0.3 In) • Weight 22 G (0.77 Oz) • Volume 12.5 Cm3 (0.76 In3 ) • Surface Area 47.3 Cm2 (7.33 In2 ) • Materials And Substances To Which The Patient Can Be Exposed B C D E F Titanium, Polyurethane, Silicone, Silicone Medical Adhesive • Power Sourceg 1.2 Amp Hours, 3.2 V Lithium, Fluorinated Carbon – Silver Vanadium Oxide Hybrid • Expected Lifetime 10.2, Spinal Cord Stimulation Implants: Implantable Neurostimulation System Is Indicated For Spinal Cord Stimulation (scs) As An Aid In The Management Of Chronic, Intractable Pain Of The Trunk And/or Limbs - Including Unilateral Or Bilateral Pain. • Fully Implantable Spinal Cord Neurostimulator • ~1 Hour Recharge — Empty To Full (approximate Time) • Technology Automatically Adjusts The Therapy As Your Patient Moves, Delivering A Personalized Treatment Based On Seven Unique Body Positions. • Physicians To Objectively Monitor A Patients Progress. • Ergonomic Features: • Weight : Approx.29.1g (1.0oz) • Height : Approx. 57.1mm (2.2in) • Width: Approx. 47.2mm (1.9in) • Battery Type : Rechargeable • Volume : Approx. 13.9 Cc • Technology Should Be Optimized For The Increased Energy Demands Of Hd Therapies. • Technology Should Give Patients The Broadest Access To Mri* Because It Allows Mri Scans Anywhere On The Body, Under Certain Conditions. • >95% Battery Capacity Retained At 9 Years, Independent Of Therapy Parameters Or Recharge Preferences • Ability To Recharge A Completely Discharged Device Using Recharger. • Easy-to-adjust Therapy Using Programmer. • Easy-to-read Interface, Percutaneous Leads : • Subcompact Eight Electrode Lead. • Lead Must Have 8 Contacts. • Contact Length Should Be Approx. : 3.0 Mm • Contact Spacing Should Be Approx. : 1.5 Mm • Lead Length Approx. : 75 Cm • Lead Kit Must Have Bent Stylet , Straight Stylet, Passing Straw, Guide Wire, Tunneling Tip, Tunneling Rod, 14 Ga 3.5" Tuohy Needle , 14 Ga 3.5" Tuohy Curved Tip Needle And Anchor With Anchor Dispenser Tool. Extension : • Should Be Approx.. 60 Cm In Length • Extension Should Have 8 Contacts. • Extension Kit Must Have 1 × 8 Extension Boots, Clear, 1 × 8 Extension Boots, White Set Screw, Approx.. 38 Cm Passer, Tunneling Obturator, Torque Wrench. Surgical Lead : • 16-contact Paddle Lead ( 5-6-5) • Approx.. Size : 10.0 Mm Wide, 2.0 Mm Thick, 65 Cm Length • Lead Kit Must Have :, A) Passing Elevator, B) Lead Blank, C) Tunneling Tool, D) Tunneling Tool Tip, E) Passing Straw, F) Torque Wrench, G) 1 × 8 Extension Boots, Intrathecal Programmable Pump : Itp Is Implantable Infusion System Delivers Drug Directly Into The Intrathecal Space, Thereby Bypassing The Blood-brain Barrier. As A Result, Only A Fraction Of The Oral Dose Is Needed To Eliminate Systemic Opioids, Sustain Pain Relief Produce Efficacy While Minimizing Systemic Side Effects. Features: Pump Should Offer In Two Sizes (20 Ml Or 40 Ml) To Create Efficient Refill Intervals. Powerful Long-lasting Durability With Diamond-like Carbon Coating That Resists The Wear From Gear Revolutions Designed To Last Up To Seven Years At Up To 0.9 Ml/day Flow Rate ±0.3% Repeatability — Each Pump Precisely Delivers A Reliable And Consistent Amount Of Drug‡ Allows Safe Full-body Access To 1.5- And 3.0-tesla Mri. The Pump Must Be Designed To Resume Programmed Therapy After The Scan And Does Not Need To Be Emptied Prior To A Scan, Minimizing Drug Waste And Procedural Steps. Pump Has Catheter Access Port, Catheter Port, Suture Loop, Reservoir Fill Port. The Pump Should Be Programmed To Vary The Amount Of Medication Up To 13 Different Times Throughout A Day. Programming Can Also Vary From Day To Day. The Pump Should Store Important Data About The Device And Settings, So It Is Not Needed To Carry Records If Patient Travels Or Change Clinics. The Information Should Be Accessible With A Clinician Programming Device. The Pump Should Allow For Full Body Mri Scans Under Specific Conditions., Dural Patch * Should Be Made Up Of Material Poly-l-lactic Acid To Provide The Biocompatibility & Non Toxicity. * Should Be Hydrophobic To Provide Water Light Barrier For The Prevention Of Csf Leakage. * Should Provide The Bio Mimetic Structure Which Resembles To The Microstructure Of Native Dural Matrix, Providing An Appropriate Environment For Dural Cell Growth. * Should Be Absorbable Within 6 Months. * Should Be Sutured And Onlay On To The Dural Defect. * Should Be Available As Pre Sterilised By Gama Radiation. * Thickness Should Be From 0.1-0.5 Mm. * Should Be Available In Sizes In Mm As, 15x20mm, 20x30mm, 30x40mm, 40x60mm, 60x60mm, 60x80mm, Burr Hole Bone Void Filler/scaffold Designed To Perfectly Fit Into Burr Holes, Allows Easy Handling. Does Not Require Additional Fixation. The Plug Should Have Option To Use Along With A Drain Or Shunt Size Of Plug Corresponds To The Perforator Size. Should Have Sizes Ranging From 8mm To 15mm(with 1mm Increment) 3d Printed – Fused Deposition Modelling Method, Prints Layer By Layer. Tissue Friendly Material, Not A Permanent Implant, Reduce Risks Of Infection, Reduce Risks Of Long- Term Morbidity. Degrades In The Body 18-24 Months – Via Hydrolysis. Open Pore System: Visible Pores From The Side And Top Of The Scaffold – This Is To Facilitate Rapid Vascularization. Each Layer Is Printed At An Angle To The Previous - Cancellous Bone Graft Revascularization Occurs Rapidly Because Of Its Open Microarchitecture. Scaffold Structure - Porous Interconnected Micro-architecture That Demonstrates Mechanical Properties Similar To Human Cancellous Bone. Should Be A Radiolucent Material Visible To Access Bone In-growth Should Come In Sterile Pack Sterile By Gamma Irradiation, In A Single Layer Foil Packaging. Shelf Life – 2years, Craniotomy Bone Void Filler/ Scaffold- It Should Be A Press And Fit Scaffold To Fill The Bone Gaps Along With The Craniotomy Flap. Is Flexible And Easily Contoured To Fit In The Gap Should Be Available In Different Sizes To Fit The Craniotomy Gaps 3d Printed – Fused Deposition Modelling Method, Prints Layer By Layer. Tissue Friendly Material, Not A Permanent Implant, Reduce Risks Of Infection, Reduce Risks Of Long- Term Morbidity. 7degrades In The Body 18-24 Months – Via Hydrolysis. Open Pore System: Visible Pores From The Side And Top Of The Scaffold – This Is To Facilitate Rapid Vascularization. Each Layer Is Printed At An Angle To The Previous - Cancellous Bone Graft Revascularization Occurs Rapidly Because Of Its Open Microarchitecture. Scaffold Structure - Porous Interconnected Micro-architecture That Demonstrates Mechanical Properties Similar To Human Cancellous Bone. Should Be A Radiolucent Material Visible To Access Bone In-growth Should Come In Sterile Pack Sterile By Gamma Irradiation, In A Single Layer Foil Packaging. Shelf Life – 2years All Implant Should Made Of Titanium/mri Compatible Material & Should Be Of Same Company Any Make For A Single Surgery Construct. All Various Sizes Of Implants Should Be Compatible/fitted In The System Of The Bidders Implant. All Various Instruments Needed For Fitting The Implants Should Be Supplied By Bidder Prior To The Surgery. Implant Should Be U.s. Fda/four Digit Europen Ce/cdsco Certified. Bidder Should Have Provide Clinical Studies With Minimum Three Year Follow Up. Bidder Should Have Provide Satisfaction Letter From Well Recognized Government Institutes. Like Aiims/pgi/sgpgi/cmc Veuore/or Equivalent Institute, Bone Void Filler/scaffold Should Be A Semi-rigid Bone Filler. Should Be Malleable And Easily Contoured Using Warm Sterile Water Or Saline Easy To Cut With Surgical Scissors And Easy To Trim With Surgical Blade. Should Be Available In Different Sizes And Thickness 3d Printed – Fused Deposition Modelling Method, Prints Layer By Layer. Tissue Friendly Material, Not A Permanent Implant, Reduce Risks Of Infection, Reduce Risks Of Long- Term Morbidity. Degrades In The Body 18-24 Months – Via Hydrolysis. Open Pore System: Visible Pores From The Side And Top Of The Scaffold – This Is To Facilitate Rapid Vascularization. Each Layer Is Printed At An Angle To The Previous - Cancellous Bone Graft Revascularization Occurs Rapidly Because Of Its Open Microarchitecture.scaffold Structure - Porous Interconnected Micro-architecture That Demonstrates Mechanical Properties Similar To Human Cancellous Bone. Should Be A Radiolucent Material Visible To Access Bone In-growth Should Come In Sterile Pack Sterile By Gamma Irradiation, In A Single Layer Foil Packaging. Shelf Life – 2years