Modular Hybrid Glenoid SSI002562

GUDID 00887868229268

Shoulder glenoid fossa prosthesis trial

Primary Device ID	00887868229268
NIH Device Record Key	d073ad82-b995-4cdf-8e3b-034b315e7f44
Commercial Distribution Status	In Commercial Distribution
Brand Name	Modular Hybrid Glenoid
Version Model Number	SSI002562
Catalog Number	SSI002562
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	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

Phone	1 (800) 343-9500
Email	customerservice@zimmerbiomet.com

Device Size Text, specify

Device Issuing Agency	Device ID
GS1	00887868229268 [Primary]

KWT	Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented

Steralize Prior To Use	true
Device Is Sterile	false

[00887868229268]

Moist Heat or Steam Sterilization