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Aprikos

EUDAMED

Class I (EU MDR)

Ref AM03-257-23

by Aprikos Medical AS

Identity

Trade Name
Aprikos EUDAMED
Device Name
LP-24_Genral_Surgery_Forceps EUDAMED
Model / Reference
AM03-257-23 EUDAMED

Identifiers

Primary DI / UDI-DI
07073371012104 EUDAMED
Basic UDI-DI
7073371FILENO24X3 EUDAMED
Direct Marketing DI
07073371012104 EUDAMED
EMDN Code
L031399 GENERAL SURGERY FORCEPS, REUSABLE - OTHER 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 4018d890-3374-4d7f-8c94-6f4d9cbb47e4 61 fields · synced Jun 20, 2026