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Aprikos Medical

EUDAMED

Class I (EU MDR)

Ref AM19-111-01

by Aprikos Medical AS

Identity

Trade Name
Aprikos Medical EUDAMED
Device Name
Vaginal Speculum EUDAMED
Model / Reference
AM19-111-01 EUDAMED

Identifiers

Primary DI / UDI-DI
07073371091031 EUDAMED
Basic UDI-DI
7073371FILE101L7 EUDAMED
Direct Marketing DI
07073371091031 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

Category: Vaginal speculum, reusable

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

Similar devices

Also classified as Vaginal speculum, reusable.

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 20adae34-88ef-4771-83ef-e9e87bdfe47e 61 fields · synced Jun 18, 2026