Home GUDID 00816127021282 iNSitu™ Hip System
Primary DI 00816127021282
Brand iNSitu™ Hip System
Company NEXTSTEP ARTHROPEDIX, LLC
Model 10-86-3652
Device description Hooded Liner Trial Size 52 x 36mm ID
Published 2023-08-31
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true Product Codes# Code, Name table Code Name LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented OQG Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented OQI Hip, Semi-Constrained, Cemented, Metal/Ceramic/Polymer + Additive, Porous Uncemented
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented Orthopedic 2 LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented Orthopedic 2 OQG Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented Orthopedic 2 OQI Hip, Semi-Constrained, Cemented, Metal/Ceramic/Polymer + Additive, Porous Uncemented Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00816127021282 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00816127021282 00816127021282 816127021282 0816127021282
GMDN Terms# Term, Definition table Term Definition Acetabulum prosthesis trial, prefabricated, reusable A copy of a final acetabular prosthesis designed to be used for trial reductions during hip arthroplasty to judge the correct size and position of the final acetabular prosthesis to be implanted. It is one of a set, or a set, of graduated sizes, is typically made of metal or polymer material and may be designed in the form of cages, shells, augments, or inserts. This is a reusable device intended to be sterilized prior to use.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 060211165 Device count 1 DM exempt true Lot or batch true Sterilization required before use true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00816127025518 TheRay Collared and Collarless Femoral Stem 12-12-0000 2025-09-02 00816127025525 TheRay Collared and Collarless Femoral Stem 12-12-0001 2025-09-02 00816127025532 TheRay Collared and Collarless Femoral Stem 12-12-0002 2025-09-02 00816127025549 TheRay Collared and Collarless Femoral Stem 12-12-0003 2025-09-02 00816127025556 TheRay Collared and Collarless Femoral Stem 12-12-0004 2025-09-02 00816127025563 TheRay Collared and Collarless Femoral Stem 12-12-0005 2025-09-02 00816127025570 TheRay Collared and Collarless Femoral Stem 12-12-0006 2025-09-02 00816127025587 TheRay Collared and Collarless Femoral Stem 12-12-0007 2025-09-02 00816127025594 TheRay Collared and Collarless Femoral Stem 12-12-0008 2025-09-02 00816127025600 TheRay Collared and Collarless Femoral Stem 12-12-0009 2025-09-02 00816127025617 TheRay Collared and Collarless Femoral Stem 12-12-0010 2025-09-02 00816127025648 TheRay Collared and Collarless Femoral Stem 12-13-0000 2025-09-02 00816127025655 TheRay Collared and Collarless Femoral Stem 12-13-0001 2025-09-02 00816127025662 TheRay Collared and Collarless Femoral Stem 12-13-0002 2025-09-02 00816127025679 TheRay Collared and Collarless Femoral Stem 12-13-0003 2025-09-02 00816127025686 TheRay Collared and Collarless Femoral Stem 12-13-0004 2025-09-02 00816127025693 TheRay Collared and Collarless Femoral Stem 12-13-0005 2025-09-02 00816127025709 TheRay Collared and Collarless Femoral Stem 12-13-0006 2025-09-02 00816127025716 TheRay Collared and Collarless Femoral Stem 12-13-0007 2025-09-02 00816127025723 TheRay Collared and Collarless Femoral Stem 12-13-0008 2025-09-02
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