Hemasorb Plus

GUDID 00850391007009

ABYRX, INC.

Bone wax, synthetic

• Primary Device ID: 00850391007009
• NIH Device Record Key: 5ca97408-7739-41b3-a4b1-f2a462c708b5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hemasorb Plus
• Version Model Number: HPS-311-NS
• Company DUNS: 078818942
• Company Name: ABYRX, INC.
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850391007009 [Primary]

FDA Product Code

• MTJ: Wax,Bone

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-12-15

On-Brand Devices [Hemasorb Plus]

• 00850391007108: HPS-811-NS
• 00850391007009: HPS-311-NS