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Aprikos Medical

EUDAMED

Class I (EU MDR)

Ref AM19-121-01

by Aprikos Medical AS

Identity

Trade Name
Aprikos Medical EUDAMED
Device Name
Vaginal Speculum EUDAMED
Model / Reference
AM19-121-01 EUDAMED

Identifiers

Primary DI / UDI-DI
07073371091369 EUDAMED
Basic UDI-DI
7073371FILE101L7 EUDAMED
Direct Marketing DI
07073371091369 EUDAMED
EMDN Code
L059001 VAGINAL SPECULUMS, 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 Medical 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 5963f8f0-3b57-4f17-b78a-e6d6035664ea 61 fields · synced Jun 19, 2026