AGC ANATOMIC FEMORAL PROVISIONAL 32-467339

GUDID 05019279494170

Biomet Uk Ltd

Knee femur prosthesis trial, reusable

• Primary Device ID: 05019279494170
• NIH Device Record Key: 87dac29a-c880-4236-85a8-12d4cf6b809d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AGC ANATOMIC FEMORAL PROVISIONAL
• Version Model Number: 32-467339
• Catalog Number: 32-467339
• 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	05019279494170 [Primary]

FDA Product Code

• HWT: TEMPLATE

Sterilization

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

[05019279494170]

Moist Heat or Steam Sterilization

[05019279494170]

Moist Heat or Steam Sterilization

[05019279494170]

Moist Heat or Steam Sterilization

[05019279494170]

Moist Heat or Steam Sterilization

[05019279494170]

Moist Heat or Steam Sterilization

[05019279494170]

Moist Heat or Steam Sterilization

[05019279494170]

Moist Heat or Steam Sterilization

[05019279494170]

Moist Heat or Steam Sterilization

[05019279494170]

Moist Heat or Steam Sterilization

[05019279494170]

Moist Heat or Steam Sterilization

[05019279494170]

Moist Heat or Steam Sterilization

[05019279494170]

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 ANATOMIC FEMORAL PROVISIONAL]

• 05019279494279: 32-467348
• 05019279494255: 32-467346
• 05019279494231: 32-467344
• 05019279494217: 32-467342
• 05019279494194: 32-467340
• 05019279494156: 32-467338
• 05019279494132: 32-467336
• 05019279494118: 32-467334
• 05019279494095: 32-467332
• 05019279494071: 32-467330
• 05019279494293: 32-467349
• 05019279494170: 32-467339