Home GUDID 05019279861941 AGC TIBIAL PUNCH
Primary DI 05019279861941
Brand AGC TIBIAL PUNCH
Company Biomet Uk Ltd
Model 32-467284
Catalog number 32-467284
Published 2017-07-28
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile false
Single use false Product Codes# Code, Name table Code Name HWP PUNCH, FEMORAL NECK
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class HWP Punch, Femoral Neck Orthopedic 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 05019279861941 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 05019279861941 05019279861941 5019279861941
GMDN Terms# Term, Definition table Term Definition Bone punch, reusable A hand-held manual surgical instrument with a cutting/biting action used to cut small cross-sectional pieces of bone typically for biopsy or fixation procedures during a surgical intervention. It is typically designed with a long, thin, two-part sliding shaft (the upper part sliding along the lower part) which is joined to sprung (self-opening), pivoted, pistol grip handles. The working end terminates with a sharp, angled, cutting jaw that closes over an endpiece when the handles are squeezed together cutting through the bone. It is available in various sizes and designs (e.g., it can have upward or downward located jaws) and is made of high-grade stainless steel. This is a reusable device.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 219322575 Device count 1 DM exempt false Premarket exempt true HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label false Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 05019279477333 Oxford Partial Knee SystemFemoral Impactor 32-420127 32-420127 2020-05-23 05019279905638 OXFORD UNICOMPARTMENTAL KNEE PHASE 3TIBIAL IMPACTOR 32-420932 32-420932 2020-05-23 05019279439935 Oxford® Partial Knee System 32-422974 32-422974 2020-05-23 05019279439942 Oxford® Partial Knee System 32-422975 32-422975 2020-05-23 05019279439959 Oxford® Partial Knee System 32-422976 32-422976 2020-05-23 00880304525672 Oxford® Partial Knee System 32-422097 32-422097 2025-01-10 00887868259050 Oxford® Partial Knee System 110031779 110031779 2025-01-10 00887868354694 Oxford® Partial Knee System 166570 166570 2025-01-10 00887868354700 Oxford® Partial Knee System 166571 166571 2025-01-10 00887868354717 Oxford® Partial Knee System 166572 166572 2025-01-10 00887868354724 Oxford® Partial Knee System 166573 166573 2025-01-10 00887868354731 Oxford® Partial Knee System 166574 166574 2025-01-10 00887868354748 Oxford® Partial Knee System 166575 166575 2025-01-10 00887868354755 Oxford® Partial Knee System 166576 166576 2025-01-10 00887868354762 Oxford® Partial Knee System 166577 166577 2025-01-10 00887868354779 Oxford® Partial Knee System 166578 166578 2025-01-10 00887868354786 Oxford® Partial Knee System 166579 166579 2025-01-10 00887868354793 Oxford® Partial Knee System 166580 166580 2025-01-10 00887868354809 Oxford® Partial Knee System 166581 166581 2025-01-10 00887868354816 Oxford® Partial Knee System 166845 166845 2025-01-10
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