PSN A-Ref 4 In 1 W/SLTS SSI005826

GUDID 00889024588158

Zimmer, Inc.

Orthopaedic prosthesis implantation instrument, reusable

• Primary Device ID: 00889024588158
• NIH Device Record Key: b315e46f-47d0-4773-88b1-97c13369ef95
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PSN A-Ref 4 In 1 W/SLTS
• Version Model Number: SSI005826
• Catalog Number: SSI005826
• 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	00889024588158 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K142787

FDA Product Code

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

Sterilization

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

[00889024588158]

Moist Heat or Steam Sterilization

[00889024588158]

Moist Heat or Steam Sterilization

[00889024588158]

Moist Heat or Steam Sterilization

[00889024588158]

Moist Heat or Steam Sterilization

[00889024588158]

Moist Heat or Steam Sterilization

[00889024588158]

Moist Heat or Steam Sterilization

[00889024588158]

Moist Heat or Steam Sterilization

[00889024588158]

Moist Heat or Steam Sterilization

[00889024588158]

Moist Heat or Steam Sterilization

[00889024588158]

Moist Heat or Steam Sterilization

[00889024588158]

Moist Heat or Steam Sterilization

[00889024588158]

Moist Heat or Steam Sterilization

[00889024588158]

Moist Heat or Steam Sterilization

[00889024588158]

Moist Heat or Steam Sterilization

[00889024588158]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-02-26
• Device Publish Date: 2020-02-18

On-Brand Devices [PSN A-Ref 4 In 1 W/SLTS]

• 00889024588240: SSI005835
• 00889024588233: SSI005834
• 00889024588226: SSI005833
• 00889024588219: SSI005832
• 00889024588202: SSI005831
• 00889024588196: SSI005830
• 00889024588189: SSI005829
• 00889024588172: SSI005828
• 00889024588165: SSI005827
• 00889024588158: SSI005826