Home GUDID 04719872159780 U1 Hip System
Primary DI 04719872159780
Brand U1 Hip System
Company UNITED ORTHOPEDIC CORP.
Model 1201-2836
Catalog number 1201-2836
Device description Femoral head trial, φ36mm, +10mm
Published 2022-06-15
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 JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented Orthopedic 2 LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 04719872159780 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 04719872159780 04719872159780 4719872159780
GMDN Terms# Term, Definition table Term Definition Femoral head prosthesis trial A copy of a final femoral head prosthesis designed to be used for trial reductions during hip arthroplasty to judge the correct size, and to help achieve the desired offset, leg-length, and range of motion of the final prosthesis to be implanted. It is one of a set, or a set, of graduated sizes, and is used in conjunction with femoral stem trial or final prostheses; some may be used with explantation instruments during removal of implanted acetabulum cups. It is typically made of metal or polymer material and includes trial adapters used with large trial heads. This is a reusable device intended to be sterilized prior to use.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 656700556 Device count 1 Lot or batch true Manufacturing date on label true Sterilization required before use true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 10885862015181 Aura Exactech, Inc. JDI 2022-10-04 10885862015198 Aura Exactech, Inc. JDI 2022-10-04 10885862015204 Aura Exactech, Inc. JDI 2022-10-04 10885862015211 Aura Exactech, Inc. JDI 2022-10-04 10885862013743 NA Exactech, Inc. JDI 2022-09-20 10885862013743 NA Exactech, Inc. LPH 2022-09-20 10885862013750 NA Exactech, Inc. LPH 2022-09-20 10885862013750 NA Exactech, Inc. JDI 2022-09-20 10885862022448 NA Exactech, Inc. LPH 2022-09-19 10885862022448 NA Exactech, Inc. JDI 2022-09-19 10885862022455 NA Exactech, Inc. JDI 2022-09-19 10885862022455 NA Exactech, Inc. LPH 2022-09-19 10885862029867 NA Exactech, Inc. JDI 2022-09-19 10885862029867 NA Exactech, Inc. LPH 2022-09-19 10885862034038 Novation Exactech, Inc. JDI 2022-09-19 10885862034045 Novation Exactech, Inc. JDI 2022-09-19 10885862034052 Novation Exactech, Inc. JDI 2022-09-19 10885862034069 Novation Exactech, Inc. JDI 2022-09-19 10885862034076 Novation Exactech, Inc. JDI 2022-09-19 10885862034083 Novation Exactech, Inc. JDI 2022-09-19 10885862034090 Novation Exactech, Inc. JDI 2022-09-19 10885862034106 Novation Exactech, Inc. JDI 2022-09-19 10885862034113 Novation Exactech, Inc. JDI 2022-09-19 10885862033598 Novation Exactech, Inc. JDI 2022-08-25 10885862033604 Novation Exactech, Inc. JDI 2022-08-25 10885862033611 Novation Exactech, Inc. JDI 2022-08-25 10885862033628 Novation Exactech, Inc. JDI 2022-08-25 10885862033635 Novation Exactech, Inc. JDI 2022-08-25 10885862033642 Novation Exactech, Inc. JDI 2022-08-25 10885862033741 Novation Exactech, Inc. JDI 2022-08-25