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Cf-Bobath-15

EUDAMED

Class I (EU MDR)

Ref CF-BOBATH-15

by Mobercas Sl

Identity

Trade Name
CF-BOBATH-15 EUDAMED
Device Name
CF-BOBATH-15 EUDAMED
Model / Reference
CF-BOBATH-15 EUDAMED

Identifiers

Primary DI / UDI-DI
08436591371045 EUDAMED
Basic UDI-DI
843659137CF-BOBATH-15V2 EUDAMED
Direct Marketing DI
08436591371045 EUDAMED
EMDN Code
V08050101 GENERIC USE STRETCHERS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain 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

Cf-Bobath-15 by Mobercas Sl — 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
Mobercas Sl
EUDAMED SRN
ES-MF-000025078

Sources (1)

  • EUDAMED 7b9696b9-5823-407a-a48f-7ba1f73e364f 61 fields · synced Jul 14, 2026