Persona Femoral Sizer NG-Style SSI005647

GUDID 00889024584747

Zimmer, Inc.

Orthopaedic prosthesis implantation instrument, reusable

• Primary Device ID: 00889024584747
• NIH Device Record Key: dd31b0b8-7f31-4937-baeb-6c77e1552440
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Persona Femoral Sizer NG-Style
• Version Model Number: SSI005647
• Catalog Number: SSI005647
• Company DUNS: 056038268
• Company Name: Zimmer, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024584747 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K113369

FDA Product Code

• JWH: Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Sterilization

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

[00889024584747]

Moist Heat or Steam Sterilization

[00889024584747]

Moist Heat or Steam Sterilization

[00889024584747]

Moist Heat or Steam Sterilization

[00889024584747]

Moist Heat or Steam Sterilization

[00889024584747]

Moist Heat or Steam Sterilization

[00889024584747]

Moist Heat or Steam Sterilization

[00889024584747]

Moist Heat or Steam Sterilization

[00889024584747]

Moist Heat or Steam Sterilization

[00889024584747]

Moist Heat or Steam Sterilization

[00889024584747]

Moist Heat or Steam Sterilization

[00889024584747]

Moist Heat or Steam Sterilization

[00889024584747]

Moist Heat or Steam Sterilization

[00889024584747]

Moist Heat or Steam Sterilization

[00889024584747]

Moist Heat or Steam Sterilization

[00889024584747]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-02-19
• Device Publish Date: 2020-02-11

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