"2.4" FRACTURE SYSTEM 01-9172

GUDID 00841036079284

BIOMET MICROFIXATION, INC

Surgical countersink, reusable
Primary Device ID00841036079284
NIH Device Record Key88728df4-1c49-4445-8511-7fa99715f8a1
Commercial Distribution StatusIn Commercial Distribution
Brand Name"2.4" FRACTURE SYSTEM
Version Model Number01-9172
Catalog Number01-9172
Company DUNS046189866
Company NameBIOMET MICROFIXATION, INC
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(904)741-4400
EmailFXJAX-ORDERS@ZIMMERBIOMET.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS100841036079284 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00841036079284]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-04-18

On-Brand Devices ["2.4" FRACTURE SYSTEM]

0084103607928401-9172
0084103605990301-9174

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