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Soflex Electrique

EUDAMED

Class I (EU MDR)

Ref 5605.00-UKModel FAUTEUIL ELEVATEUR DE DOUCHERef 5605.00

by France Reval

Identity

Trade Name
SOFLEX ELECTRIQUE EUDAMED
Device Name
SOFLEX EUDAMED
Model / Reference
FAUTEUIL ELEVATEUR DE DOUCHE EUDAMED
5605.00-UK EUDAMED
5605.00 EUDAMED

Identifiers

Primary DI / UDI-DI
36664010014584 EUDAMED
36664010014652 EUDAMED
Basic UDI-DI
3666401DC006JZ EUDAMED
Direct Marketing DI
36664010014652 EUDAMED
EMDN Code
Y093399 WASHING, BATHING AND SHOWERING DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands EUDAMED
France 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: Hydrotherapy bath/tank

Soflex Electrique by France Reval — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Hydrotherapy bath/tank.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
France Reval
EUDAMED SRN
FR-MF-000011523

Sources (2)

  • EUDAMED 09ccdb02-621e-451c-a0c4-ced04b2731c6 61 fields · synced Jul 31, 2026
  • EUDAMED 96b18df8-4fb3-4a3d-ada0-5ee2581af550 61 fields · synced May 19, 2026