BIOMET SERIES A 32-484788

GUDID 00880304438026

Biomet Orthopedics, LLC

Patella prosthesis trial
Primary Device ID00880304438026
NIH Device Record Key5c408c79-50d8-42a6-8664-bba29e339527
Commercial Distribution StatusIn Commercial Distribution
Brand NameBIOMET SERIES A
Version Model Number32-484788
Catalog Number32-484788
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 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.com

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100880304438026 [Primary]

FDA Product Code

HWTTEMPLATE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00880304438026]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-05-30
Device Publish Date2017-07-28

On-Brand Devices [BIOMET SERIES A]

0088030443808832-484720
0088030443807132-484724
0088030443806432-484704
0088030443805732-484706
0088030443804032-484708
0088030443803332-484726
0088030443802632-484788
0088030443801932-484786
0088030443800232-484770
0088030443799932-484768
0088030443798232-484766
0088030443797532-484764
0088030443796832-484762
0088030443795132-484760
0088030443794432-484700
0088030443792032-484722
0088030443791332-484728
0088030443790632-484780
0088030443789032-484710
0088030443772232-484782
0088030443762332-484784

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