Femoral Head 31-476946

GUDID 00887868258886

Biomet Orthopedics, LLC

Orthopaedic implant driver

• Primary Device ID: 00887868258886
• NIH Device Record Key: 5b9851f2-cba7-421f-9fc8-3e8977d1836a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Femoral Head
• Version Model Number: 31-476946
• Catalog Number: 31-476946
• 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: 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)348-9500
• Email: customerservice@zimmerbiomet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868258886 [Primary]

FDA Product Code

• HWR: DRIVER, PROSTHESIS

Sterilization

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

[00887868258886]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-03-11
• Device Publish Date: 2019-02-15

On-Brand Devices [Femoral Head]

• 00887868268878: 31-476948
• 00887868258886: 31-476946
• 00887868569586: 31-476948