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Hero Flex

EUDAMED

Class I (EU MDR)

Ref 5001015

by Open Bionics Ltd.

Identity

Trade Name
Hero Flex EUDAMED
Device Name
Hero Flex EUDAMED
Model / Reference
5001015 EUDAMED

Identifiers

Primary DI / UDI-DI
05060639240418 EUDAMED
Basic UDI-DI
506063924HEROFLEXV9 EUDAMED
Direct Marketing DI
05060639240418 EUDAMED
EMDN Code
P090299,P090399,P090499 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

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

Hero Flex by Open Bionics Ltd. — 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

Manufacturer
Open Bionics Ltd.
EUDAMED SRN
GB-MF-000032650
Authorised Representative
European Healthcare & Device Solutions Ltd. IE-AR-000003999

Sources (1)

  • EUDAMED 5f4e3bf7-e76d-4742-97da-70937baa3906 61 fields · synced Jul 8, 2026