Identity
- Trade Name
- NovaBone Putty Syringe EUDAMED
- Device Name
- NovaBone Putty Syringe EUDAMED
- Model / Reference
- 771605 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 00813909010175 EUDAMED
- Basic UDI-DI
- B-00813909010175 EUDAMED
- EMDN Code
- P900401 BONE AND TENDON REPLACEMENT DEVICES EUDAMED
Classification
- Device Class
- Class III EUDAMED
- Market of Registration
- Greece EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
Yes
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
NovaBone Putty Syringe by NovaBone Products, LLC — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-00813909010175 | Class III | Active |
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Manufacturer
- Manufacturer
- NovaBone Products, LLC
- EUDAMED SRN
- US-MF-000020624
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (1)
- EUDAMED 5a9748e8-8b2c-49b4-bb9e-5139ca7be50c 61 fields · synced Jun 9, 2026