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Aprikos

EUDAMED

Class I (EU MDR)

Ref AM12-145-06

by Aprikos Medical AS

Identity

Trade Name
Aprikos EUDAMED
Device Name
LP-30 Osteotomes EUDAMED
Model / Reference
AM12-145-06 EUDAMED

Identifiers

Primary DI / UDI-DI
07073371034168 EUDAMED
Basic UDI-DI
7073371FILENO30WW EUDAMED
Direct Marketing DI
07073371034168 EUDAMED
EMDN Code
L090401 ORTHOPAEDIC SURGERY OSTEOTOMES, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Norway EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Aprikos by Aprikos Medical AS — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Aprikos Medical AS
EUDAMED SRN
NO-MF-000044411

Sources (1)

  • EUDAMED 19f06bc2-647c-4da0-98fd-7c1c3ad3ba42 61 fields · synced Jun 19, 2026