OPTIVAC TOTAL HIP KIT 418000

GUDID 00880304370647

BIOMET

Orthopaedic cement preparation/delivery kit

• Primary Device ID: 00880304370647
• NIH Device Record Key: cfdf0890-8d02-40c9-b354-42837a745169
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OPTIVAC TOTAL HIP KIT
• Version Model Number: 418000
• Catalog Number: 418000
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00880304370647 [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 TOTAL HIP KIT]

• 00880304370647: 418000
• 00880304370562: 417000