COPELAND EAS SHOULDER SYSTEM 11-114662

GUDID 00880304439931

Biomet Orthopedics, LLC

Resurfacing humeral head prosthesis

• Primary Device ID: 00880304439931
• NIH Device Record Key: 9bdb966a-8c06-4be0-82f4-8be4eb72972d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: COPELAND EAS SHOULDER SYSTEM
• Version Model Number: 11-114662
• Catalog Number: 11-114662
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304439931 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K051843

FDA Product Code

• HSD: PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-10-24

On-Brand Devices [COPELAND EAS SHOULDER SYSTEM]

• 00880304439962: 11-114668
• 00880304439955: 11-114666
• 00880304439948: 11-114661
• 00880304439931: 11-114662
• 00880304439924: 11-114664
• 00880304439917: 11-114667
• 00880304439900: 11-114663
• 00880304439894: 11-114665