AGC JIG REMOVAL INSTRUMENT 32-467296

GUDID 05019279493937

Biomet Uk Ltd

Orthopaedic implant inserter/extractor, reusable
Primary Device ID05019279493937
NIH Device Record Keyed682de5-8a44-49da-b3ef-ed17ab2a30c2
Commercial Distribution StatusIn Commercial Distribution
Brand NameAGC JIG REMOVAL INSTRUMENT
Version Model Number32-467296
Catalog Number32-467296
Company DUNS219322575
Company NameBiomet Uk Ltd
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.c

Device Identifiers

Device Issuing AgencyDevice ID
GS105019279493937 [Primary]

FDA Product Code

HXXSCREWDRIVER

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[05019279493937]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-04-23
Device Publish Date2017-07-28

Devices Manufactured by Biomet Uk Ltd

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05019279438884 - Oxford® Partial Knee System2023-07-06
05019279150366 - Oxford® Instruments2023-05-03
05019279465972 - MAXIM KNEE INSTRUMENTATION2023-05-03
05019279466238 - AGC Knee System2023-05-03
05019279466887 - MAXIM KNEE INSTRUMENTATION2023-05-03
05019279467266 - MAXIM KNEE INSTRUMENTATION2023-05-03
05019279490004 - OXFORD UNICOMPARTMENTAL KNEE PHASE 3TIBIAL RESECTOR HEADLESS NAIL2023-05-03

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