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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

Forté Flex Crème — Class I MDD by Fysioline Oy

MD Atlas
Fysioline Oy

EUDAMED last updated this device on Sep 9, 2025

Forté Flex Crème

B-3700221303641MC

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Fysioline Oy
UDI-DI code: D-3700221303641MC
Reference / catalog number: 800_547

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Manufacturer information

Organization name: Fysioline Oy
SRN: FI-MF-000001173
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW011
Mise en garde: Ne pas appliquer sur les muqueuses, dans les yeux et les plaies ouvertes. Tenir hors de la portée des enfants. Déconseillé aux femmes enceintes et allaitantes, ainsi qu'aux enfants de moins de 2 ans. Uniquement pour usage externe.

Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: Forté Flex Crème
UDI-DI code: D-3700221303641MC
Basic UDI-DI: B-3700221303641MC
Reference / catalog number: 800_547
Issuing entity: EUDAMED

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Forté Flex Crème articulations est une crème topique contenant du sulfate de chondroïtine, de l'acide hyaluronique et du menthol. La formulation spécifique de Forté Flex Crème articulations convient au traitement d'appoint des douleurs articulaires, des entorses, des foulures et des sollicitations excessives. Soulage rapidement et efficacement la douleur et réduit l'inflammation. Agit également sur les ecchymoses et atténue les gonflements.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 100 MU03

EMDN nomenclature code(s)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.