MP TIBIAL TRAY CRUCIATE PUNCH 32-484525

GUDID 00880304612204

Biomet Orthopedics, LLC

Bone punch, reusable
Primary Device ID00880304612204
NIH Device Record Keyec2af162-9ac1-4e4b-826d-eacfd04ca851
Commercial Distribution StatusIn Commercial Distribution
Brand NameMP TIBIAL TRAY CRUCIATE PUNCH
Version Model Number32-484525
Catalog Number32-484525
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
GS100880304612204 [Primary]

FDA Product Code

HWPPUNCH, FEMORAL NECK

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00880304612204]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-07-28

On-Brand Devices [MP TIBIAL TRAY CRUCIATE PUNCH]

0088030461222832-484527
0088030461221132-484526
0088030461220432-484525
0088030461219832-484524
0088030461218132-484523
0088030461217432-484522
0088030461216732-484521

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