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Bond Apatite

EUDAMED

Class III (EU MDR)

Ref HA-BB-LAA

by Augma Biomaterials

Identity

Trade Name
Bond Apatite EUDAMED
Device Name
Bond Apatite EUDAMED
Model / Reference
HA-BB-LAA EUDAMED

Identifiers

Primary DI / UDI-DI
07290014838109 EUDAMED
Basic UDI-DI
B-07290014838109 EUDAMED
EMDN Code
Q010302 DENTAL GRAFT DEVICES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
France 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

Bond Apatite by Augma Biomaterials — 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

Manufacturer
Augma Biomaterials
EUDAMED SRN
IL-MF-000020802
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED bd0bb406-a6c9-4301-9c78-4880e31ca978 61 fields · synced Jun 18, 2026