Persona® The Personalized Knee® System 97-5026-250-00

GUDID 00887868554360

Zimmer, Inc.

Surgical implant template, reusable

• Primary Device ID: 00887868554360
• NIH Device Record Key: fa01bc2b-b06b-4d2f-9708-46dab59eb6ad
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Persona® The Personalized Knee® System
• Version Model Number: 97-5026-250-00
• Catalog Number: 97-5026-250-00
• Company DUNS: 056038268
• Company Name: Zimmer, Inc.
• 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: true
• 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: true

Customer Support Contacts

• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@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 Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868554360 [Primary]

FDA Product Code

• HWT: TEMPLATE

Sterilization

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

[00887868554360]

Moist Heat or Steam Sterilization

[00887868554360]

Moist Heat or Steam Sterilization

[00887868554360]

Moist Heat or Steam Sterilization

[00887868554360]

Moist Heat or Steam Sterilization

[00887868554360]

Moist Heat or Steam Sterilization

[00887868554360]

Moist Heat or Steam Sterilization

[00887868554360]

Moist Heat or Steam Sterilization

[00887868554360]

Moist Heat or Steam Sterilization

[00887868554360]

Moist Heat or Steam Sterilization

[00887868554360]

Moist Heat or Steam Sterilization

[00887868554360]

Moist Heat or Steam Sterilization

[00887868554360]

Moist Heat or Steam Sterilization

[00887868554360]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-12-01
• Device Publish Date: 2022-11-23

On-Brand Devices [Persona® The Personalized Knee® System]

• 00887868554360: 97-5026-250-00
• 00889024632257: 110046018
• 00889024632240: 110046017
• 00889024632233: 42-5099-044-52
• 00889024650572: 110047401
• 00889024650565: 110047400
• 00889024650558: 110047399
• 00889024646490: 42-5903-070-00