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CopiOs Bone Void Filler - Sponge 5cc
EUDAMEDFDA UDIClass III (EU MDR)
Ref 07.00582.003Model CB00030
Identity
- Trade Name
- CopiOs Bone Void Filler - Sponge 5cc EUDAMEDCopiOs® Bone Void Filler Sponge FDA UDI
- Generic Name
- Bone matrix implant, composite FDA UDI
- Device Name
- CopiOs Bone Void Filler - Sponge EUDAMEDSponge FDA UDI
- Model / Reference
- CB00030 EUDAMED07.00582.003 EUDAMED20100-02 FDA UDI
- Description
- Sponge FDA UDI
Identifiers
- Catalog Number
- 07.00582.003 FDA UDI
- Primary DI / UDI-DI
- 00812337021029 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00812337021029 EUDAMED
- FDA Product Code
- MQV FDA UDI
- EMDN Code
- P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED
- GMDN Term
- Bone matrix implant, composite FDA UDI
Classification
- Device Class
- Class III EUDAMEDClass II FDA UDI
- Regulation Number
- 888.3045 FDA UDI
- Market of Registration
- Italy EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
Yes
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 5 Milliliter FDA UDI
CopiOs Bone Void Filler - Sponge 5cc by Dsm Biomedical, Inc. — Class III — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-00812337021029 | Class III | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
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Manufacturer
- Manufacturer
- DSM Biomedical, Inc.
- EUDAMED SRN
- US-MF-000021393
- Authorised Representative
- DSM Biomedical B.V. NL-AR-000018633
Sources (2)
- EUDAMED ad800ec8-239e-42c3-8996-11d72ab4855f 61 fields · synced Jun 18, 2026
- FDA UDI 74f2f865-dd8f-44e5-9a3b-ece245930b32 35 fields · synced May 29, 2026