CORB®

GUDID 00889024066175

Zimmer, Inc.

Orthopaedic prosthesis implantation instrument, reusable

• Primary Device ID: 00889024066175
• NIH Device Record Key: 066f710a-ae43-451b-b995-7e30e850c6ee
• Commercial Distribution Discontinuation: 2017-05-19
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: CORB®
• Version Model Number: 3240-13
• 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: true
• Serial Number: false
• 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)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmer.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024066175 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K811005

FDA Product Code

• HSZ: INSTRUMENT, SURGICAL, ORTHOPEDIC, PNEUMATIC POWERED & ACCESSORY/ATTACHMENT

Sterilization

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

[00889024066175]

Moist Heat or Steam Sterilization

[00889024066175]

Moist Heat or Steam Sterilization

[00889024066175]

Moist Heat or Steam Sterilization

[00889024066175]

Moist Heat or Steam Sterilization

[00889024066175]

Moist Heat or Steam Sterilization

[00889024066175]

Moist Heat or Steam Sterilization

[00889024066175]

Moist Heat or Steam Sterilization

[00889024066175]

Moist Heat or Steam Sterilization

[00889024066175]

Moist Heat or Steam Sterilization

[00889024066175]

Moist Heat or Steam Sterilization

[00889024066175]

Moist Heat or Steam Sterilization

[00889024066175]

Moist Heat or Steam Sterilization

[00889024066175]

Moist Heat or Steam Sterilization

[00889024066175]

Moist Heat or Steam Sterilization

[00889024066175]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-07-02

On-Brand Devices [CORB®]

• 00889024066328: 3240-65
• 00889024066311: 3240-64
• 00889024066304: 3240-63
• 00889024066298: 3240-62
• 00889024066267: 3240-43
• 00889024066250: 3240-42
• 00889024066243: 3240-41
• 00889024066236: 3240-33
• 00889024066229: 3240-32
• 00889024066212: 3240-31
• 00889024066205: 3240-23
• 00889024066199: 3240-22
• 00889024066182: 3240-21
• 00889024066175: 3240-13
• 00889024066168: 3240-12
• 00889024066151: 3240-11
• 00889024066144: 3240-01