BIO PLUG 163025

GUDID 00880304255142

Biomet Orthopedics, LLC

Polymer orthopaedic cement restrictor, non-bioabsorbable, sterile
Primary Device ID00880304255142
NIH Device Record Key6b42b0fb-c33f-4d83-88d1-2c57b45dec55
Commercial Distribution StatusIn Commercial Distribution
Brand NameBIO PLUG
Version Model Number163025
Catalog Number163025
Company DUNS129278169
Company NameBiomet Orthopedics, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
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
GS100880304255142 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JDSNAIL, FIXATION, BONE

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-10-24

On-Brand Devices [BIO PLUG]

00880304255142163025
00880304004108163020
00880304004092163010
00880304004085163015
00880304004078163005

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