Home GUDID 04048844693510 implaFit®
Primary DI 04048844693510
Brand implaFit®
Company implantcast GmbH
Model 80091003
Device description short stem with collar cementless lateralized
Published 2026-03-26
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile true
Single use true Product Codes# Code, Name table Code Name KWY Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented MEH Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented Orthopedic 2 LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented Orthopedic 2 MEH Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 04048844693510 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 04048844693510 04048844693510 4048844693510
GMDN Terms# Term, Definition table Term Definition Press-fit femoral stem prosthesis A sterile implantable device designed to replace the proximal femoral neck as part of a total hip arthroplasty (THA). The device is contoured to enable fixation by pressing the distal end into the cortex of the remaining natural femur to achieve a mechanical interlock without the use of bone cement. The device is made of metal [e.g., cobalt-chrome (Co-Cr), titanium (Ti), stainless steel].
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0
Regulatory Flags# DUNS number 324369826 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 10885862653697 Alteon Exactech, Inc. MEH 2026-05-26 10885862653703 Alteon Exactech, Inc. MEH 2026-05-26 10885862653710 Alteon Exactech, Inc. MEH 2026-05-26 10885862653727 Alteon Exactech, Inc. MEH 2026-05-26 10885862653734 Alteon Exactech, Inc. MEH 2026-05-26 10885862653741 Alteon Exactech, Inc. MEH 2026-05-26 10885862653758 Alteon Exactech, Inc. MEH 2026-05-26 10885862653765 Alteon Exactech, Inc. MEH 2026-05-26 10885862653772 Alteon Exactech, Inc. MEH 2026-05-26 10885862653789 Alteon Exactech, Inc. MEH 2026-05-26 10885862653796 Alteon Exactech, Inc. MEH 2026-05-26 10885862653802 Alteon Exactech, Inc. MEH 2026-05-26 10885862653819 Alteon Exactech, Inc. MEH 2026-05-26 10885862653826 Alteon Exactech, Inc. MEH 2026-05-26 10885862653833 Alteon Exactech, Inc. MEH 2026-05-26 10885862653840 Alteon Exactech, Inc. MEH 2026-05-26 10885862653857 Alteon Exactech, Inc. MEH 2026-05-26 10885862653864 Alteon Exactech, Inc. MEH 2026-05-26 10885862653871 Alteon Exactech, Inc. MEH 2026-05-26 10885862653888 Alteon Exactech, Inc. MEH 2026-05-26 10885862653895 Alteon Exactech, Inc. MEH 2026-05-26 10885862653901 Alteon Exactech, Inc. MEH 2026-05-26 10885862653918 Alteon Exactech, Inc. MEH 2026-05-26 10885862653925 Alteon Exactech, Inc. MEH 2026-05-26 10885862653932 Alteon Exactech, Inc. MEH 2026-05-26 10885862653949 Alteon Exactech, Inc. MEH 2026-05-26 10885862653956 Alteon Exactech, Inc. MEH 2026-05-26 10885862653963 Alteon Exactech, Inc. MEH 2026-05-26 10885862653970 Alteon Exactech, Inc. MEH 2026-05-26 10885862653987 Alteon Exactech, Inc. MEH 2026-05-26