Vanguard M Series Knee 32-423117

GUDID 05019279442126

Biomet Uk Ltd

Knee tibia prosthesis trial, reusable

• Primary Device ID: 05019279442126
• NIH Device Record Key: 91d6b809-7fb4-472c-ab40-363c3ff9d312
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vanguard M Series Knee
• Version Model Number: 32-423117
• Catalog Number: 32-423117
• Company DUNS: 219322575
• Company Name: Biomet Uk Ltd
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	05019279442126 [Primary]

FDA Product Code

• HWT: TEMPLATE

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[05019279442126]

Moist Heat or Steam Sterilization

[05019279442126]

Moist Heat or Steam Sterilization

[05019279442126]

Moist Heat or Steam Sterilization

[05019279442126]

Moist Heat or Steam Sterilization

[05019279442126]

Moist Heat or Steam Sterilization

[05019279442126]

Moist Heat or Steam Sterilization

[05019279442126]

Moist Heat or Steam Sterilization

[05019279442126]

Moist Heat or Steam Sterilization

[05019279442126]

Moist Heat or Steam Sterilization

[05019279442126]

Moist Heat or Steam Sterilization

[05019279442126]

Moist Heat or Steam Sterilization

[05019279442126]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-03-22
• Device Publish Date: 2020-05-23

On-Brand Devices [Vanguard M Series Knee]

• 05019279442232: 32-423124
• 05019279442218: 32-423123
• 05019279442201: 32-423122
• 05019279442188: 32-423121
• 05019279442171: 32-423120
• 05019279442157: 32-423119
• 05019279442140: 32-423118
• 05019279442126: 32-423117
• 05019279442119: 32-423116
• 05019279442102: 32-423115
• 05019279442089: 32-423114
• 05019279442072: 32-423113
• 05019279442065: 32-423112
• 05019279442041: 32-423111
• 05019279442034: 32-423110
• 05019279442027: 32-423109
• 05019279442003: 32-423108
• 05019279441990: 32-423107
• 05019279441983: 32-423106
• 05019279441969: 32-423105
• 05019279441952: 32-423104
• 05019279441938: 32-423103
• 05019279441921: 32-423102
• 05019279441365: 32-423101