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NovaBone Putty MIS

EUDAMED

Class III (EU MDR)

Ref 772610Ref 772605

by NovaBone Products, LLC

Identity

Trade Name
NovaBone Putty MIS EUDAMED
Device Name
NovaBone Putty MIS EUDAMED
Model / Reference
772610 EUDAMED
772605 EUDAMED

Identifiers

Primary DI / UDI-DI
00813909010229 EUDAMED
00813909010212 EUDAMED
Basic UDI-DI
B-00813909010229 EUDAMED
B-00813909010212 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 MIS 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 9ef76e51-fa20-4611-9f8c-ae685828614a 61 fields · synced Jul 17, 2026
  • EUDAMED e5f27077-e78c-48a9-90c2-318bd8ed154a 61 fields · synced May 16, 2026