AGC PS FEMORAL PROVISIONAL 32-468026

GUDID 05019279495979

Biomet Uk Ltd

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• Primary Device ID: 05019279495979
• NIH Device Record Key: db540d2e-a74e-4cbe-a495-66401261ccdb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AGC PS FEMORAL PROVISIONAL
• Version Model Number: 32-468026
• Catalog Number: 32-468026
• 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	05019279495979 [Primary]

FDA Product Code

• HWT: TEMPLATE

Sterilization

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

[05019279495979]

Moist Heat or Steam Sterilization

[05019279495979]

Moist Heat or Steam Sterilization

[05019279495979]

Moist Heat or Steam Sterilization

[05019279495979]

Moist Heat or Steam Sterilization

[05019279495979]

Moist Heat or Steam Sterilization

[05019279495979]

Moist Heat or Steam Sterilization

[05019279495979]

Moist Heat or Steam Sterilization

[05019279495979]

Moist Heat or Steam Sterilization

[05019279495979]

Moist Heat or Steam Sterilization

[05019279495979]

Moist Heat or Steam Sterilization

[05019279495979]

Moist Heat or Steam Sterilization

[05019279495979]

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 PS FEMORAL PROVISIONAL]

• 05019279495771: 32-468012
• 05019279495757: 32-468011
• 05019279495979: 32-468026
• 05019279495955: 32-468025
• 05019279495931: 32-468024
• 05019279495917: 32-468023
• 05019279495894: 32-468022
• 05019279495870: 32-468021
• 05019279495856: 32-468016
• 05019279495832: 32-468015
• 05019279495818: 32-468014
• 05019279495795: 32-468013