AGC V2 MILLENNIUM INSTRUMENT 32-468451

GUDID 05019279496730

Biomet Uk Ltd

Knee femur prosthesis trial, reusable Knee femur prosthesis trial, reusable Knee femur prosthesis trial, reusable Knee femur prosthesis trial, reusable Knee femur prosthesis trial, reusable Knee femur prosthesis trial, reusable Knee femur prosthesis trial, reusable Knee femur prosthesis trial, reusable Knee femur prosthesis trial, reusable Knee femur prosthesis trial, reusable Knee femur prosthesis trial, reusable Knee femur prosthesis trial, reusable
Primary Device ID05019279496730
NIH Device Record Key85300af4-49a6-4bf2-99f3-60fd7471ada8
Commercial Distribution StatusIn Commercial Distribution
Brand NameAGC V2 MILLENNIUM INSTRUMENT
Version Model Number32-468451
Catalog Number32-468451
Company DUNS219322575
Company NameBiomet Uk Ltd
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

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
GS105019279496730 [Primary]

FDA Product Code

HWTTEMPLATE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[05019279496730]

Moist Heat or Steam Sterilization


[05019279496730]

Moist Heat or Steam Sterilization


[05019279496730]

Moist Heat or Steam Sterilization


[05019279496730]

Moist Heat or Steam Sterilization


[05019279496730]

Moist Heat or Steam Sterilization


[05019279496730]

Moist Heat or Steam Sterilization


[05019279496730]

Moist Heat or Steam Sterilization


[05019279496730]

Moist Heat or Steam Sterilization


[05019279496730]

Moist Heat or Steam Sterilization


[05019279496730]

Moist Heat or Steam Sterilization


[05019279496730]

Moist Heat or Steam Sterilization


[05019279496730]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2022-03-22
Device Publish Date2020-05-23

On-Brand Devices [AGC V2 MILLENNIUM INSTRUMENT]

0501927949683932-468456
0501927949671632-468446
0501927949370832-467261
0501927949500932-467602
0501927949673032-468451
0501927949373932-467263

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