LINER IMPACTOR PLATE 423637

GUDID 00880304371965

Biomet Orthopedics, LLC

Orthopaedic implant impactor
Primary Device ID00880304371965
NIH Device Record Keyc7b0c0a4-abfa-4601-baa3-31a710e34ea6
Commercial Distribution StatusIn Commercial Distribution
Brand NameLINER IMPACTOR PLATE
Version Model Number423637
Catalog Number423637
Company DUNS129278169
Company NameBiomet Orthopedics, LLC
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(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
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.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 Identifiers

Device Issuing AgencyDevice ID
GS100880304371965 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00880304371965]

Moist Heat or Steam Sterilization


[00880304371965]

Moist Heat or Steam Sterilization


[00880304371965]

Moist Heat or Steam Sterilization


[00880304371965]

Moist Heat or Steam Sterilization


[00880304371965]

Moist Heat or Steam Sterilization


[00880304371965]

Moist Heat or Steam Sterilization


[00880304371965]

Moist Heat or Steam Sterilization


[00880304371965]

Moist Heat or Steam Sterilization


[00880304371965]

Moist Heat or Steam Sterilization


[00880304371965]

Moist Heat or Steam Sterilization


[00880304371965]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-07-28

On-Brand Devices [LINER IMPACTOR PLATE]

00880304371972423638
00880304371965423637
00880304371958423636
00880304371941423635
00880304371934423634
00880304371927423633
00880304371910423632
00880304371903423631
00880304371897423630

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