HYBRID GLENOID 406150

GUDID 00880304456365

Biomet Orthopedics, LLC

Wire cutter

• Primary Device ID: 00880304456365
• NIH Device Record Key: d5d440ee-5004-4d34-9de3-ba1c34097f4b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HYBRID GLENOID
• Version Model Number: 406150
• Catalog Number: 406150
• 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	00880304456365 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[00880304456365]

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 [HYBRID GLENOID]

• 00880304462625: 113952
• 00880304462618: 113956
• 00880304462489: 113954
• 00880304462472: 113951
• 00880304459854: PT-113950
• 00880304456600: 406152
• 00880304456587: 406151
• 00880304456570: 406182
• 00880304456457: 406181
• 00880304456365: 406150
• 00887868343865: 113951
• 00887868261169: SSI002443
• 00887868261152: SSI002442