← Back to catalogue

Ce-2150-Abr

EUDAMED

Class I (EU MDR)

Ref CE-2150-ABR

by Mobercas Sl

Identity

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

Identifiers

Primary DI / UDI-DI
08436591370734 EUDAMED
Basic UDI-DI
843659137CE-2150-ABRWZ EUDAMED
Direct Marketing DI
08436591370734 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-Abr 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Mobercas Sl
EUDAMED SRN
ES-MF-000025078

Sources (1)

  • EUDAMED d45ba3d0-1d2d-4e3b-adfe-589e8481d3eb 61 fields · synced Jul 9, 2026