SCP® PF Knee Kit 464303

GUDID 00889024501270

ZIMMER KNEE CREATIONS, INC.

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• Primary Device ID: 00889024501270
• NIH Device Record Key: d300a2b4-336e-4f33-a4e1-def669c657a7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SCP® PF Knee Kit
• Version Model Number: 464303
• Catalog Number: 464303
• Company DUNS: 078836317
• Company Name: ZIMMER KNEE CREATIONS, 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.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 Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024501270 [Primary]
GS1	00889024501270 [Primary]
GS1	00889024501270 [Primary]
GS1	00889024501270 [Primary]
GS1	00889024501270 [Primary]
GS1	00889024501270 [Primary]
GS1	00889024501270 [Primary]
GS1	00889024501270 [Primary]
GS1	00889024501270 [Primary]
GS1	00889024501270 [Primary]
GS1	00889024501270 [Primary]
GS1	00889024501270 [Primary]
GS1	00889024501270 [Primary]
GS1	00889024501270 [Primary]
GS1	00889024501270 [Primary]

FDA Product Code

• OJH: Orthopedic tray
• OJH: Orthopedic tray
• OJH: Orthopedic tray
• OJH: Orthopedic tray
• OJH: Orthopedic tray
• OJH: Orthopedic tray
• OJH: Orthopedic tray
• OJH: Orthopedic tray
• OJH: Orthopedic tray
• OJH: Orthopedic tray
• OJH: Orthopedic tray
• OJH: Orthopedic tray
• OJH: Orthopedic tray
• OJH: Orthopedic tray
• OJH: Orthopedic tray

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-06-17
• Device Publish Date: 2020-06-09

On-Brand Devices [SCP® PF Knee Kit]

• 00889024501294: 464503
• 00889024501287: 464502
• 00889024501270: 464303