OXFORD UNI KNEE SYSTEM 32-422831

GUDID 05019279401550

Biomet Uk Ltd

Surgical implant template, reusable
Primary Device ID05019279401550
NIH Device Record Key5f362184-afb8-4cb0-91ee-41b01e626d9a
Commercial Distribution StatusIn Commercial Distribution
Brand NameOXFORD UNI KNEE SYSTEM
Version Model Number32-422831
Catalog Number32-422831
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 Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS105019279401550 [Primary]

FDA Product Code

HWTTEMPLATE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[05019279401550]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-06-26
Device Publish Date2017-07-28

On-Brand Devices [OXFORD UNI KNEE SYSTEM]

0501927940377632-422843
0501927940375232-422842
0501927940184032-422838
0501927940182632-422837
0501927940179632-422836
0501927940176532-422835
0501927940160432-422834
0501927940158132-422833
0501927940157432-422832
0501927940155032-422831
0501927944811132-423242
0501927944809832-423240
0501927944806732-423238
0501927944804332-423236
0501927944801232-423234
0088030450471432-422845

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