DFS ANTERIOR ANGULAR HINGE 06185

GUDID 00887868083549

Biomet Orthopedics, LLC

External orthopaedic fixation system, single-use, non-sterile
Primary Device ID00887868083549
NIH Device Record Keya4a33fb8-a149-4706-831a-fcff32366a7e
Commercial Distribution StatusIn Commercial Distribution
Brand NameDFS ANTERIOR ANGULAR HINGE
Version Model Number06185
Catalog Number06185
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

Device Size Text, specify0
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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
GS100887868083549 [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

[00887868083549]

Moist Heat or Steam Sterilization


[00887868083549]

Moist Heat or Steam Sterilization


[00887868083549]

Moist Heat or Steam Sterilization


[00887868083549]

Moist Heat or Steam Sterilization


[00887868083549]

Moist Heat or Steam Sterilization


[00887868083549]

Moist Heat or Steam Sterilization


[00887868083549]

Moist Heat or Steam Sterilization


[00887868083549]

Moist Heat or Steam Sterilization


[00887868083549]

Moist Heat or Steam Sterilization


[00887868083549]

Moist Heat or Steam Sterilization


[00887868083549]

Moist Heat or Steam Sterilization


[00887868083549]

Moist Heat or Steam Sterilization


[00887868083549]

Moist Heat or Steam Sterilization


[00887868083549]

Moist Heat or Steam Sterilization


[00887868083549]

Moist Heat or Steam Sterilization


[00887868083549]

Moist Heat or Steam Sterilization


[00887868083549]

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 ANTERIOR ANGULAR HINGE]

0088786808354906185
0088786808352506180
0088786808350106175
0088786808348806165
0088786808347106160
0088786808346406150

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