RESORBABLE SCREW SYSTEM 950012

GUDID 00880304416154

Biomet Orthopedics, LLC

Surgical depth gauge, reusable

• Primary Device ID: 00880304416154
• NIH Device Record Key: cb1b17e6-6144-4dd1-9bb7-c37f2f4e674e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RESORBABLE SCREW SYSTEM
• Version Model Number: 950012
• Catalog Number: 950012
• 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	00880304416154 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[00880304416154]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-06-19
• Device Publish Date: 2019-06-11

On-Brand Devices [RESORBABLE SCREW SYSTEM]

• 00880304416246: 950044
• 00880304416161: 950025
• 00880304416154: 950012
• 70880304416733: 951548