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Um-Cuf-Ks-La-Kc

EUDAMED

Class I (EU MDR)

Ref CUF-KS-LAModel A0925 CUF-KS-LA

by A&D Company, Limited

Identity

Device Name
UM-CUF-KS-LA-KC EUDAMED
Model / Reference
A0925 CUF-KS-LA EUDAMED
CUF-KS-LA EUDAMED

Identifiers

Primary DI / UDI-DI
05060006582516 EUDAMED
Basic UDI-DI
4981046-CFA2516-36 EUDAMED
EMDN Code
Z1203020302 NON–INVASIVE BLOOD PRESSURE MONITORING INSTRUMENTS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Greece 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

Um-Cuf-Ks-La-Kc by A&D Company, Limited — 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

EUDAMED SRN
JP-MF-000002158
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 4dc76fe8-ac7e-4e7f-8672-2cb027087d0d 61 fields · synced Jun 19, 2026