DFS® Mini Lengthener 07035

GUDID 00887868358166

Biomet Orthopedics, LLC

External orthopaedic fixation system, single-use, non-sterile
Primary Device ID00887868358166
NIH Device Record Key5d0ff286-a1ae-4214-ba21-703b00242be1
Commercial Distribution StatusIn Commercial Distribution
Brand NameDFS® Mini Lengthener
Version Model Number07035
Catalog Number07035
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
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Device Size Text, specify0
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Device Identifiers

Device Issuing AgencyDevice ID
GS100887868358166 [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

[00887868358166]

Moist Heat or Steam Sterilization


[00887868358166]

Moist Heat or Steam Sterilization


[00887868358166]

Moist Heat or Steam Sterilization


[00887868358166]

Moist Heat or Steam Sterilization


[00887868358166]

Moist Heat or Steam Sterilization


[00887868358166]

Moist Heat or Steam Sterilization


[00887868358166]

Moist Heat or Steam Sterilization


[00887868358166]

Moist Heat or Steam Sterilization


[00887868358166]

Moist Heat or Steam Sterilization


[00887868358166]

Moist Heat or Steam Sterilization


[00887868358166]

Moist Heat or Steam Sterilization


[00887868358166]

Moist Heat or Steam Sterilization


[00887868358166]

Moist Heat or Steam Sterilization


[00887868358166]

Moist Heat or Steam Sterilization


[00887868358166]

Moist Heat or Steam Sterilization


[00887868358166]

Moist Heat or Steam Sterilization


[00887868358166]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-09-30
Device Publish Date2019-09-20

On-Brand Devices [DFS® Mini Lengthener]

0088786835822707065
0088786835819707050
0088786835817307037
0088786835816607035
0088786835815907030

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