Home GUDID 04048266003751 IntraBlock™ TwinStem™
Primary DI 04048266003751
Brand IntraBlock™ TwinStem™
Company Merete GmbH
Model size 12.50 Standard
Catalog number HR35012
Device description IntraBlock™ TwinStem™ non-cemented size 12.50 Standard 12/14 TiAl6V4 ELI TPS-Coating sterile
Published 2017-01-01
Public version status Update
Distribution status Not 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 LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 04048266003751 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 04048266003751 04048266003751 4048266003751
GMDN Terms# Term, Definition table Term Definition Coated hip femur prosthesis, modular A sterile implantable principal component of a total hip prosthesis (femoral component) designed to replace the femoral head and neck; the device is composed of two or more separate pieces (e.g., head, neck, and stem) designed to be joined and is coated with a material (e.g., porous materials, hydroxyapatite) intended to improve fixation and stability by promoting bone ingrowth. The device may be made of metal and/or ceramic materials. Fixation devices for implantation (e.g., screws and bolts) may be included and implantation may be performed with or without bone cement.
Regulatory Flags# DUNS number 313267265 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 04048844693367 implaFit® implantcast GmbH LZO 2026-03-26 04048844693411 implaFit® implantcast GmbH LZO 2026-03-26 04048844693442 implaFit® implantcast GmbH LZO 2026-03-26 04048844693510 implaFit® implantcast GmbH LZO 2026-03-26 04048844693565 implaFit® implantcast GmbH LZO 2026-03-26 04048844693596 implaFit® implantcast GmbH LZO 2026-03-26 04048844731977 implaFit® implantcast GmbH LZO 2026-03-20 04048844732042 implaFit® implantcast GmbH LZO 2026-03-20 04048844732059 implaFit® implantcast GmbH LZO 2026-03-20 04048844732080 implaFit® implantcast GmbH LZO 2026-03-20 04048844732097 implaFit® implantcast GmbH LZO 2026-03-20 10885862660145 N/A Exactech, Inc. LZO 2026-03-19 10885862660152 N/A Exactech, Inc. LZO 2026-03-19 10885862660169 N/A Exactech, Inc. LZO 2026-03-19 10885862660176 N/A Exactech, Inc. LZO 2026-03-19 10885862660183 N/A Exactech, Inc. LZO 2026-03-19 10885862660190 N/A Exactech, Inc. LZO 2026-03-19 10885862660206 N/A Exactech, Inc. LZO 2026-03-19 10885862660213 N/A Exactech, Inc. LZO 2026-03-19 10885862660220 N/A Exactech, Inc. LZO 2026-03-19 10885862660237 N/A Exactech, Inc. LZO 2026-03-19 10885862660244 N/A Exactech, Inc. LZO 2026-03-19 10885862660251 N/A Exactech, Inc. LZO 2026-03-19 10885862660268 N/A Exactech, Inc. LZO 2026-03-19 10885862660275 N/A Exactech, Inc. LZO 2026-03-19 10885862660282 N/A Exactech, Inc. LZO 2026-03-19 10885862660299 N/A Exactech, Inc. LZO 2026-03-19 10885862660305 N/A Exactech, Inc. LZO 2026-03-19 10885862660312 N/A Exactech, Inc. LZO 2026-03-19 10885862660329 N/A Exactech, Inc. LZO 2026-03-19