AGC MODULAR TIBIAL II 32-349025

GUDID 00880304330276

Biomet Orthopedics, LLC

Surgical implant template, reusable
Primary Device ID00880304330276
NIH Device Record Key50c4c0c3-c89f-4345-8cb6-323c4fbb84bc
Commercial Distribution StatusIn Commercial Distribution
Brand NameAGC MODULAR TIBIAL II
Version Model Number32-349025
Catalog Number32-349025
Company DUNS129278169
Company NameBiomet Orthopedics, LLC
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 Datetrue
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.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100880304330276 [Primary]

FDA Product Code

HWTTEMPLATE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00880304330276]

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 [AGC MODULAR TIBIAL II]

0088030434182132-468421
0088030434180732-468419
0088030434176032-468414
0088030434174632-468412
0088030434173932-468411
0088030434166132-468403
0088030434165432-468401
0088030433028332-349026
0088030433027632-349025
0088030433026932-349024
0088030433025232-349023
0088030433024532-349022
0088030400413932-468402
0088030434172232-468410
0088030434343632-470190
0088030434337532-470170
0088030434221732-468522
0088030434164732-468400
0088030434152432-468387
0088030434177732-468416
0088030434171532-468409
0088030434218732-468512

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