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Fortuna

EUDAMED

Class I (EU MDR)

Ref EX1102XLModel EX110A

by Fortuna Healthcare Limited

Identity

Trade Name
FORTUNA EUDAMED
Device Name
NEOPRENE ANKLE SUPPORT EUDAMED
Model / Reference
EX110A EUDAMED
EX1102XL EUDAMED

Identifiers

Primary DI / UDI-DI
05031720000624 EUDAMED
Basic UDI-DI
5031720EX110AAF EUDAMED
EMDN Code
Y06120601 PASSIVE ANKLE-FOOT ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland 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: Ankle/foot orthosis

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

Similar devices

Also classified as Ankle/foot orthosis.

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 2599e766-6dba-4789-8ea0-85811d6dcc53 61 fields · synced Jun 18, 2026