1.5/2.0MM CMF SYSTEM RACK

GUDID 00841036274504

BIOMET MICROFIXATION, INC

Surgical instrument/implant rack

• Primary Device ID: 00841036274504
• NIH Device Record Key: 1e472b5e-24e3-49dc-8e98-1a59638a14ba
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 1.5/2.0MM CMF SYSTEM RACK
• Version Model Number: 15-1153
• Company DUNS: 046189866
• Company Name: BIOMET MICROFIXATION, 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: 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(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: 1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: 1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: 1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: 1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: 1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: 1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: 1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: 1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: 1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: 1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: 1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: 1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: 1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: 1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: 1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: 1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841036274504 [Primary]

FDA Product Code

• JEY: Plate, Bone

Sterilization

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

[00841036274504]

Moist Heat or Steam Sterilization

[00841036274504]

Moist Heat or Steam Sterilization

[00841036274504]

Moist Heat or Steam Sterilization

[00841036274504]

Moist Heat or Steam Sterilization

[00841036274504]

Moist Heat or Steam Sterilization

[00841036274504]

Moist Heat or Steam Sterilization

[00841036274504]

Moist Heat or Steam Sterilization

[00841036274504]

Moist Heat or Steam Sterilization

[00841036274504]

Moist Heat or Steam Sterilization

[00841036274504]

Moist Heat or Steam Sterilization

[00841036274504]

Moist Heat or Steam Sterilization

[00841036274504]

Moist Heat or Steam Sterilization

[00841036274504]

Moist Heat or Steam Sterilization

[00841036274504]

Moist Heat or Steam Sterilization

[00841036274504]

Moist Heat or Steam Sterilization

[00841036274504]

Moist Heat or Steam Sterilization

[00841036274504]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-06-11
• Device Publish Date: 2024-06-03

On-Brand Devices [1.5/2.0MM CMF SYSTEM RACK]

• 00841036032388: 15-1150
• 00841036274504: 15-1153