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Ce-2150-Abrpc

EUDAMED

Class I (EU MDR)

Ref CE-2150-ABRPC

by Mobercas Sl

Identity

Trade Name
CE-2150-ABRPC EUDAMED
Device Name
CE-2150-ABRPC EUDAMED
Model / Reference
CE-2150-ABRPC EUDAMED

Identifiers

Primary DI / UDI-DI
08436591370741 EUDAMED
Basic UDI-DI
843659137CE-2150-ABRPCYC EUDAMED
Direct Marketing DI
08436591370741 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

Ce-2150-Abrpc 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 4568af32-18b0-472a-ac8a-7bf4e6dd017f 61 fields · synced Jul 20, 2026