Gamma-bsm ®

GUDID 00889024205482

Etex Corporation

Synthetic bone graft

• Primary Device ID: 00889024205482
• NIH Device Record Key: 3d7add86-3ca1-4d1a-94c7-2e1e0c0ae917
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Gamma-bsm ®
• Version Model Number: 76-6010
• Company DUNS: 622221141
• Company Name: Etex Corporation
• 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: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 877-383-9276
• Email: sales@etexcorp.com

Device Dimensions

• Total Volume: 10 Milliliter

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store at 15-25 Degrees Celcius Keep Dry Keep Away From Sunlight

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024205482 [Primary]

FDA Product Code

• MQV: Filler, Bone Void, Calcium Compound

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-07-10
• Device Publish Date: 2015-10-24

On-Brand Devices [Gamma-bsm ®]

• 00889024205499: 76-6040
• 00889024205482: 76-6010
• 00889024205475: 76-6005
• 00889024205468: 76-6023
• 00889024205451: 76-6001