COMPREHENSIVE(R) SHOULDER SYSTEM 406994

GUDID 00880304009592

Biomet Orthopedics, LLC

Bone approximation clamp

• Primary Device ID: 00880304009592
• NIH Device Record Key: 4fac6c5a-1b89-4f54-ae5b-9d05cc2f63cd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: COMPREHENSIVE(R) SHOULDER SYSTEM
• Version Model Number: 406994
• Catalog Number: 406994
• 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	00880304009592 [Primary]

FDA Product Code

• GDJ: CLAMP, SURGICAL, GENERAL & PLASTIC SURGERY

Sterilization

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

[00880304009592]

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 [COMPREHENSIVE(R) SHOULDER SYSTEM]

• 00880304431904: 31-406901
• 00880304367029: 406997
• 00880304367005: 406995
• 00880304009592: 406994