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Fortuna

EUDAMED

Class I (EU MDR)

Ref FT1000XLModel FT1000

by Fortuna Healthcare Limited

Identity

Trade Name
FORTUNA EUDAMED
Device Name
ELASTICATED KNEE SUPPORT EUDAMED
Model / Reference
FT1000 EUDAMED
FT1000XL EUDAMED

Identifiers

Primary DI / UDI-DI
05031720010081 EUDAMED
Basic UDI-DI
5031720FT10008B EUDAMED
EMDN Code
Y061209 KNEE ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

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

Fortuna by Fortuna Healthcare Limited — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
UK-MF-000048072
Authorised Representative
Fortuna Healthcare (Ireland) Limited IE-AR-000044547

Sources (1)

  • EUDAMED 5308ac25-9cfb-435e-9588-448c4d7e8843 61 fields · synced Jun 11, 2026