LMH 62001012

GUDID 00889797025645

WRIGHT MEDICAL TECHNOLOGY, INC.

Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable Surgical implant template, reusable
Primary Device ID00889797025645
NIH Device Record Keyeaa3e4b1-cbb8-452c-a537-712f522a99ad
Commercial Distribution StatusIn Commercial Distribution
Brand NameLMH
Version Model Number62001012
Catalog Number62001012
Company DUNS807201207
Company NameWRIGHT MEDICAL TECHNOLOGY, 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 Datetrue
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)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com
Phone+1(800)238-7117
Emailcustomerservice@wmt.com

Device Dimensions

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 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
GS100889797025645 [Primary]

FDA Product Code

KWDPROSTHESIS, TOE, HEMI-, PHALANGEAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00889797025645]

Moist Heat or Steam Sterilization


[00889797025645]

Moist Heat or Steam Sterilization


[00889797025645]

Moist Heat or Steam Sterilization


[00889797025645]

Moist Heat or Steam Sterilization


[00889797025645]

Moist Heat or Steam Sterilization


[00889797025645]

Moist Heat or Steam Sterilization


[00889797025645]

Moist Heat or Steam Sterilization


[00889797025645]

Moist Heat or Steam Sterilization


[00889797025645]

Moist Heat or Steam Sterilization


[00889797025645]

Moist Heat or Steam Sterilization


[00889797025645]

Moist Heat or Steam Sterilization


[00889797025645]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2022-05-16
Device Publish Date2016-09-17

On-Brand Devices [LMH]

0084042017221162101003
0084042017220462101002
0084042017219862101001
00840420168054LMH-0003
00840420168047LMH-0002
00840420168030LMH-0001
0088979702560762001000
0088979702568362001023
0088979702567662001022
0088979702566962001021
0088979702565262001013
0088979702564562001012
0088979702563862001011
00889797025621Impactor
00889797025614Broach

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