← Back to catalogue

Aprikos Medical

EUDAMED

Class I (EU MDR)

Ref AM19-115-02

by Aprikos Medical AS

Identity

Trade Name
Aprikos Medical EUDAMED
Device Name
Vaginal Speculum EUDAMED
Model / Reference
AM19-115-02 EUDAMED

Identifiers

Primary DI / UDI-DI
07073371091185 EUDAMED
Basic UDI-DI
7073371FILE101L7 EUDAMED
Direct Marketing DI
07073371091185 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Aprikos Medical AS
EUDAMED SRN
NO-MF-000044411

Sources (1)

  • EUDAMED d46f3425-d476-46a9-bcda-a47c4966e6e4 61 fields · synced Jun 20, 2026