DFS MINI EXTERNAL FIXATION SYSTEM M25-04520T

GUDID 00887868104497

Biomet Orthopedics, LLC

External orthopaedic fixation system, single-use, non-sterile
Primary Device ID00887868104497
NIH Device Record Key95fac9e2-867e-4554-a70e-74aa92c3e8d7
Commercial Distribution StatusIn Commercial Distribution
Brand NameDFS MINI EXTERNAL FIXATION SYSTEM
Version Model NumberM25-04520T
Catalog NumberM25-04520T
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 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
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

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Device Identifiers

Device Issuing AgencyDevice ID
GS100887868104497 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KTTAPPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887868104497]

Moist Heat or Steam Sterilization


[00887868104497]

Moist Heat or Steam Sterilization


[00887868104497]

Moist Heat or Steam Sterilization


[00887868104497]

Moist Heat or Steam Sterilization


[00887868104497]

Moist Heat or Steam Sterilization


[00887868104497]

Moist Heat or Steam Sterilization


[00887868104497]

Moist Heat or Steam Sterilization


[00887868104497]

Moist Heat or Steam Sterilization


[00887868104497]

Moist Heat or Steam Sterilization


[00887868104497]

Moist Heat or Steam Sterilization


[00887868104497]

Moist Heat or Steam Sterilization


[00887868104497]

Moist Heat or Steam Sterilization


[00887868104497]

Moist Heat or Steam Sterilization


[00887868104497]

Moist Heat or Steam Sterilization


[00887868104497]

Moist Heat or Steam Sterilization


[00887868104497]

Moist Heat or Steam Sterilization


[00887868104497]

Moist Heat or Steam Sterilization


Device Entry Metadata

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

On-Brand Devices [DFS MINI EXTERNAL FIXATION SYSTEM]

00887868104565M30-07030T
00887868104541M30-07025T
00887868104534M30-07020T
00887868104527M30-06025T
00887868104510M30-06020T
00887868104503M30-05018T
00887868104497M25-04520T
00887868104480M25-04015T
00887868104466M30-06030T
00887868104459M16-07015

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