FIBULA COMPOSITE PLATE TRIAL 816307007

GUDID 00887868445842

Biomet Orthopedics, LLC

Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable
Primary Device ID00887868445842
NIH Device Record Key1d609942-139e-4037-b424-45588dcdc7f2
Commercial Distribution StatusIn Commercial Distribution
Brand NameFIBULA COMPOSITE PLATE TRIAL
Version Model Number816307007
Catalog Number816307007
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
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100887868445842 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887868445842]

Moist Heat or Steam Sterilization


[00887868445842]

Moist Heat or Steam Sterilization


[00887868445842]

Moist Heat or Steam Sterilization


[00887868445842]

Moist Heat or Steam Sterilization


[00887868445842]

Moist Heat or Steam Sterilization


[00887868445842]

Moist Heat or Steam Sterilization


[00887868445842]

Moist Heat or Steam Sterilization


[00887868445842]

Moist Heat or Steam Sterilization


[00887868445842]

Moist Heat or Steam Sterilization


[00887868445842]

Moist Heat or Steam Sterilization


[00887868445842]

Moist Heat or Steam Sterilization


[00887868445842]

Moist Heat or Steam Sterilization


[00887868445842]

Moist Heat or Steam Sterilization


[00887868445842]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-09-14
Device Publish Date2020-09-04

On-Brand Devices [FIBULA COMPOSITE PLATE TRIAL]

00887868046117816307014
00887868046100816307010
00887868046094816307007
00887868445866816307014
00887868445859816307010
00887868445842816307007

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