OPTIVAC KIT, 120 GRAM TRIPLE MIX 417300

GUDID 00880304370623

BIOMET

Orthopaedic cement preparation/delivery kit Orthopaedic cement preparation/delivery kit Orthopaedic cement preparation/delivery kit Orthopaedic cement preparation/delivery kit Orthopaedic cement preparation/delivery kit Orthopaedic cement preparation/delivery kit Orthopaedic cement preparation/delivery kit Orthopaedic cement preparation/delivery kit Orthopaedic cement preparation/delivery kit Orthopaedic cement preparation/delivery kit

• Primary Device ID: 00880304370623
• NIH Device Record Key: 2317a9b0-60e1-43f6-b085-d8a7ac3e27b3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OPTIVAC KIT, 120 GRAM TRIPLE MIX
• Version Model Number: 417300
• Catalog Number: 417300
• Company DUNS: 260930126
• Company Name: BIOMET
• 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: 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: +0330475759100
• Email: eufrvra@zimmerbiomet.com
• Phone: +0330475759100
• Email: eufrvra@zimmerbiomet.com
• Phone: +0330475759100
• Email: eufrvra@zimmerbiomet.com
• Phone: +0330475759100
• Email: eufrvra@zimmerbiomet.com
• Phone: +0330475759100
• Email: eufrvra@zimmerbiomet.com
• Phone: +0330475759100
• Email: eufrvra@zimmerbiomet.com
• Phone: +0330475759100
• Email: eufrvra@zimmerbiomet.com
• Phone: +0330475759100
• Email: eufrvra@zimmerbiomet.com
• Phone: +0330475759100
• Email: eufrvra@zimmerbiomet.com
• Phone: +0330475759100
• Email: eufrvra@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 Identifiers

Device Issuing Agency	Device ID
GS1	00880304370623 [Primary]

FDA Product Code

• JDZ: MIXER, CEMENT, FOR CLINICAL USE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-10-09

On-Brand Devices [OPTIVAC KIT, 120 GRAM TRIPLE MIX]

• 00880304371002: 418300
• 00880304370623: 417300