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Carexia Fpe

EUDAMED

Class I (EU MDR)

Ref FPE

by Bmb Medical

Identity

Device Name
CAREXIA FPE EUDAMED
Model / Reference
FPE EUDAMED

Identifiers

Primary DI / UDI-DI
37603459603040 EUDAMED
Basic UDI-DI
376034596FPEKT EUDAMED
Direct Marketing DI
37603459603040 EUDAMED
EMDN Code
Y122127 ELECTRIC WHEELCHAIRS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
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

Carexia Fpe by Bmb Medical — 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
Bmb Medical
EUDAMED SRN
FR-MF-000011270

Sources (1)

  • EUDAMED 738c89fb-badd-4c6c-9e71-d8684d456912 61 fields · synced Aug 1, 2026