← Back to catalogue

Harsosykerö

EUDAMED

Class I (EU MDR)

Ref 88300

by Emicaid Oy

Identity

Device Name
Harsosykerö EUDAMED
Model / Reference
88300 EUDAMED

Identifiers

Primary DI / UDI-DI
06419914002309 EUDAMED
Basic UDI-DI
64199140088958VR EUDAMED
Direct Marketing DI
06419914002309 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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: Device sterilization/disinfection container, reusable

Harsosykerö by Emicaid Oy — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, 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
Emicaid Oy
EUDAMED SRN
FI-MF-000040418

Sources (1)

  • EUDAMED 7a9433ba-9f34-462b-b1c7-86576215a9a5 61 fields · synced Jun 18, 2026