CopiOs® Bone Void Filler Sponge 00-1103-010-05

GUDID M26300110301005

DSM BIOMEDICAL, INC.

Composite bone graft

• Primary Device ID: M26300110301005
• NIH Device Record Key: 1392e564-8b00-4c0b-8f95-8f56e3054a05
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CopiOs® Bone Void Filler Sponge
• Version Model Number: 20101-02
• Catalog Number: 00-1103-010-05
• Company DUNS: 131107757
• Company Name: DSM BIOMEDICAL, 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M26300110301005 [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: 2023-06-19
• Device Publish Date: 2015-09-17

On-Brand Devices [CopiOs® Bone Void Filler Sponge]

• 00812337021067: 20101-03
• 00812337021050: 20101-02
• 00812337021043: 20101-01
• 00812337021036: 20100-03
• 00812337021029: Sponge
• 00812337021012: 20100-01
• M2630700582004: 20100-03
• M2630700582003: 20100-02
• M2630700582001: 20100-01
• M2630011301001: 20101-01
• M26300110301010: 20101-03
• M26300110301005: 20101-02