← Back to catalogue

Sulfax Magnesium

EUDAMED

Class I (EU MDR)

Ref 800_572

by Fysioline Oy

Identity

Trade Name
Sulfax Magnesium EUDAMED
Device Name
Sulfax Magnesium (50 g) EUDAMED
Model / Reference
800_572 EUDAMED

Identifiers

Primary DI / UDI-DI
06418029906151 EUDAMED
Basic UDI-DI
B-06418029906151 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Device sterilization/disinfection container, reusable

Sulfax Magnesium 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

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

Manufacturer

Manufacturer
Fysioline Oy
EUDAMED SRN
FI-MF-000001173

Sources (1)

  • EUDAMED 4ea7dc63-3b10-43c6-afd8-910810873576 61 fields · synced Jun 18, 2026