2.4MM FRACTURE SYSTEM 24-1060T

GUDID 00841036135218

BIOMET MICROFIXATION, INC

Surgical implant template, reusable
Primary Device ID00841036135218
NIH Device Record Key1d998ccb-ecfe-47ff-a376-d57ed8022ba7
Commercial Distribution StatusIn Commercial Distribution
Brand Name2.4MM FRACTURE SYSTEM
Version Model Number24-1060T
Catalog Number24-1060T
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
GS100841036135218 [Primary]

FDA Product Code

HWTTEMPLATE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00841036135218]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-09-28
Device Publish Date2018-08-28

On-Brand Devices [2.4MM FRACTURE SYSTEM]

0084103613521824-1060T
0084103607321324-1066T
0084103607293324-1068T
0084103600945801-2545

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