Home GUDID 00814703015366 Klassic HD Hooded Acetabular Insert with XLPE Poly
Primary DI 00814703015366
Brand Klassic HD Hooded Acetabular Insert with XLPE Poly
Company TOTAL JOINT ORTHOPEDICS, INC.
Model 3508.62.032
Device description Hooded Acetabular Insert with XLPE Poly, 32mm head, size 62mm
Published 2018-06-12
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Sterile true
Single use true Product Codes# Code, Name table Code Name OQG Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class OQG Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00814703015366 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 00814703015366 00814703015366 814703015366 0814703015366
GMDN Terms# Term, Definition table Term Definition Non-constrained polyethylene acetabular liner A sterile, implantable component of a two-piece acetabulum prosthesis that is inserted into an acetabular shell prosthesis to provide the articulating surface with a femoral head prosthesis as part of a total hip arthroplasty (THA). It is made of polyethylene (includes hylamer, cross-linked polyethylene), and does not include a stabilizing component to limit the range of motion of the hip.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0
Storage And Handling# Type, Low, High table Type Low High Condition Special Storage Condition, Specify 0 0 The Klassic HD Hip System should be stored in a clean, dry location at room
temperature Special Storage Condition, Specify 0 0 The Klassic HD Hip System should be stored in a clean, dry location at room temperature
Sterilization Methods# Method table Method Ethylene Oxide
Regulatory Flags# DUNS number 078416717 Device count 1 Lot or batch true Expiration date on label true Sterilization required before use true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00810094692940 AP Sizer with Short Legs SRI-10050 2026-05-15 00810094692728 CR Femoral Trial, Grit Blasted SRI-10051.01 2026-02-05 00810094692735 CR Femoral Trial, Grit Blasted SRI-10051.02 2026-02-05 00810094692742 CR Femoral Trial, Grit Blasted SRI-10051.03 2026-02-05 00810094692759 CR Femoral Trial, Grit Blasted SRI-10051.04 2026-02-05 00810094692766 CR Femoral Trial, Grit Blasted SRI-10051.05 2026-02-05 00810094692773 CR Femoral Trial, Grit Blasted SRI-10051.06 2026-02-05 00810094692780 CR Femoral Trial, Grit Blasted SRI-10051.07 2026-02-05 00810094692506 Tibial Broach Impactor, Revision 2904.00.000 2025-05-14 00810094692278 Universal Cone Impactor Head 2021.12.012 2025-04-24 00810094692285 Universal Cone Impactor Head 2021.34.018 2025-04-24 00810094692292 Universal Cone Impactor Head 2021.57.024 2025-04-24 00810094691950 Universal Cone Impactor Head, Size 1, 12° 2021.01.012 2024-09-06 00810094691967 Universa Cone Impactor Head, Size 2, 12° 2021.02.012 2024-09-06 00810094691974 Universal Cone Impactor Head, Size 3, 18° 2021.03.018 2024-09-06 00810094691981 Universal Cone Impactor Head, Size 4, 18° 2021.04.018 2024-09-06 00810094691998 Universal Cone Impactor Head, Size 5, 24° 2021.05.024 2024-09-06 00810094692001 Universal Cone Impactor Head, Size 6, 24° 2021.06.024 2024-09-06 00810094692018 Universal Cone Impactor Head, Size 7, 24° 2021.07.024 2024-09-06 00819251021197 Femoral Stem Impactor with Anteversion 1307.00.000 2023-12-11
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