KA 1MM SHIM PSN FOOT SSI007769

GUDID 00889024684249

Zimmer, Inc.

Orthopaedic prosthesis implantation positioning instrument, reusable

• Primary Device ID: 00889024684249
• NIH Device Record Key: 1337557f-0a1c-4d28-83f5-111f55d5a012
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KA 1MM SHIM PSN FOOT
• Version Model Number: SSI007769
• Catalog Number: SSI007769
• 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: false
• Serial Number: true
• 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) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• 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	00889024684249 [Primary]

FDA Product Code

• HWT: Template

Sterilization

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

[00889024684249]

Moist Heat or Steam Sterilization

[00889024684249]

Moist Heat or Steam Sterilization

[00889024684249]

Moist Heat or Steam Sterilization

[00889024684249]

Moist Heat or Steam Sterilization

[00889024684249]

Moist Heat or Steam Sterilization

[00889024684249]

Moist Heat or Steam Sterilization

[00889024684249]

Moist Heat or Steam Sterilization

[00889024684249]

Moist Heat or Steam Sterilization

[00889024684249]

Moist Heat or Steam Sterilization

[00889024684249]

Moist Heat or Steam Sterilization

[00889024684249]

Moist Heat or Steam Sterilization

[00889024684249]

Moist Heat or Steam Sterilization

[00889024684249]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-01-21
• Device Publish Date: 2025-01-13

Devices Manufactured by Zimmer, Inc.

• 00889024658134 - Persona® Knee System: 2025-02-14
• 00889024658141 - Persona® Knee System: 2025-02-14
• 00889024658158 - Persona® Knee System: 2025-02-14
• 00889024658165 - Persona® Knee System: 2025-02-14
• 00889024658172 - Persona® Knee System: 2025-02-14
• 00889024658189 - Persona® Knee System: 2025-02-14
• 00889024658196 - Persona® Knee System: 2025-02-14
• 00889024658202 - Persona® Knee System: 2025-02-14