LIGATURE WIRE 01-5818

GUDID 00841036168896

BIOMET MICROFIXATION, INC

Orthopaedic bone wire Orthopaedic bone wire
Primary Device ID00841036168896
NIH Device Record Key7e62fefa-7833-4060-a79d-0088163a287d
Commercial Distribution StatusIn Commercial Distribution
Brand NameLIGATURE WIRE
Version Model Number01-5818
Catalog Number01-5818
Company DUNS046189866
Company NameBIOMET MICROFIXATION, INC
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 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
Phone+1(904)741-4400
EmailFXJAX-ORDERS@ZIMMERBIOMET.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS100841036168896 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HTYPIN, FIXATION, SMOOTH

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00841036168896]

Moist Heat or Steam Sterilization


[00841036168896]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-11-25

On-Brand Devices [LIGATURE WIRE]

0084103626892301-5826
0084103626891601-5824
0084103616889601-5818
0084103601130701-5826
0084103601129101-5824

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