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NovaBone Putty CMF

EUDAMED

Class III (EU MDR)

Ref 770601Ref 770600

by NovaBone Products, LLC

Identity

Trade Name
NovaBone Putty CMF EUDAMED
Device Name
NovaBone Putty CMF EUDAMED
Model / Reference
770601 EUDAMED
770600 EUDAMED

Identifiers

Primary DI / UDI-DI
00813909010021 EUDAMED
00813909010014 EUDAMED
Basic UDI-DI
B-00813909010021 EUDAMED
B-00813909010014 EUDAMED
EMDN Code
Q010302 DENTAL GRAFT DEVICES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Italy 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 CMF 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

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Manufacturer

EUDAMED SRN
US-MF-000020624
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED da1a1bba-d124-4f53-b9c1-7c457113fb2a 61 fields · synced Jul 10, 2026
  • EUDAMED dfa729c2-a4e8-47f9-b7a4-40080bea3dac 61 fields · synced May 17, 2026