OSS FEMORAL AUGMENT BROACH 110018805

GUDID 00880304679818

Biomet Orthopedics, LLC

Orthopaedic broach

• Primary Device ID: 00880304679818
• NIH Device Record Key: ae47d3de-1b6c-4cd5-9ff7-46f99426b711
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OSS FEMORAL AUGMENT BROACH
• Version Model Number: 110018805
• Catalog Number: 110018805
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• 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: true
• 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)348-9500
• Email: customerservice@zimmerbiomet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304679818 [Primary]

FDA Product Code

• HTQ: BROACH

Sterilization

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

[00880304679818]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-07-28

On-Brand Devices [OSS FEMORAL AUGMENT BROACH]

• 00880304679818: 110018805
• 00880304679801: 110018804
• 00880304679795: 110018803
• 00880304679788: 110018802
• 00880304679771: 110018801