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Hialsorb Cold

EUDAMED

Class I (EU MDR)

Ref 800_540

by Fysioline Oy

Identity

Trade Name
Hialsorb Cold EUDAMED
Device Name
Hialsorb Cold EUDAMED
Model / Reference
800_540 EUDAMED

Identifiers

Primary DI / UDI-DI
08470001774798 EUDAMED
Basic UDI-DI
B-08470001774798 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Device sterilization/disinfection container, reusable

Hialsorb Cold by Fysioline Oy — Class I — MDD — 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/MDD

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Manufacturer

Manufacturer
Fysioline Oy
EUDAMED SRN
FI-MF-000001173

Sources (1)

  • EUDAMED 7864ac50-8d21-4328-b6d7-9bfe09b9e638 61 fields · synced Jun 19, 2026