ExFuse

GUDID 08809204337330

Hans Biomed Corp.

Bone matrix implant, human-derived

• Primary Device ID: 08809204337330
• NIH Device Record Key: 7be9d1ae-3b34-429f-9ad6-89569ff513f0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ExFuse
• Version Model Number: EP3
• Company DUNS: 689512625
• Company Name: Hans Biomed Corp.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: true
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: false
• Serial Number: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	08809204337330 [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: 3
• Public Version Date: 2020-07-17
• Device Publish Date: 2015-09-24

On-Brand Devices [ExFuse]

• 08809204337583: EG03
• 08809204337361: EP10
• 08809204337354: EP8
• 08809204337347: EP5
• 08809204337330: EP3
• 08809204337323: EP1
• 08809204337316: EP05
• 08809204337309: EP03
• 08809204337293: EG10
• 08809204337286: EG8
• 08809204337279: EG5
• 08809204337262: EG3
• 08809204337255: EG1
• 08809204337248: EG05