VANAGUARD DA360 SYSTEMTIBIAL TRIAL CASE 591302

GUDID 05019279451715

Biomet Uk Ltd

Instrument tray
Primary Device ID05019279451715
NIH Device Record Key4389b703-f7dc-4d22-b5af-253d1a6124fc
Commercial Distribution StatusIn Commercial Distribution
Brand NameVANAGUARD DA360 SYSTEMTIBIAL TRIAL CASE
Version Model Number591302
Catalog Number591302
Company DUNS219322575
Company NameBiomet Uk Ltd
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 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.c
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
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 Identifiers

Device Issuing AgencyDevice ID
GS105019279451715 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


[05019279451715]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-07-06
Device Publish Date2016-09-26

Devices Manufactured by Biomet Uk Ltd

00880304009387 - LINER PUSHER HEAD2024-09-11
00880304371736 - LINER PUSHER HEAD2024-09-11
05019279126354 - OXFORD PARTIAL KNEE2024-09-11
05019279129751 - OXFORD PARTIAL KNEE SYSTEMFEMORAL SLAP HAMMER2024-09-11
05019279466832 - MAXIM KNEE INSTRUMENTATION2024-09-11
05019279469246 - INTRAMEDULLARY ROD REMOVAL HOOKWITH T-HANDLE2024-09-11
05019279469444 - AGC V2 MILLENNIUM INSTRUMENT2024-09-11
05019279477234 - OXFORD UNICOMPARTMENTAL KNEE PHASE 3TRIAL FEMORAL REMOVER2024-09-11

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