AGC V2 MILLENNIUM INSTRUMENT 32-468451

GUDID 05019279496730

Biomet Uk Ltd

Knee femur prosthesis trial, reusable

• Primary Device ID: 05019279496730
• NIH Device Record Key: 85300af4-49a6-4bf2-99f3-60fd7471ada8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AGC V2 MILLENNIUM INSTRUMENT
• Version Model Number: 32-468451
• Catalog Number: 32-468451
• 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	05019279496730 [Primary]

FDA Product Code

• HWT: TEMPLATE

Sterilization

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

[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 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 [AGC V2 MILLENNIUM INSTRUMENT]

• 05019279496839: 32-468456
• 05019279496716: 32-468446
• 05019279493708: 32-467261
• 05019279495009: 32-467602
• 05019279496730: 32-468451
• 05019279493739: 32-467263
• 05019279469444: 32-401122