← Back to catalogue

Um-Lars2m1kec

EUDAMED

Class I (EU MDR)

Ref UM-LARS2M1KEC

by A&D Company, Limited

Identity

Device Name
UM-LARS2M1KEC EUDAMED
Model / Reference
UM-LARS2M1KEC EUDAMED

Identifiers

Primary DI / UDI-DI
05060006582202 EUDAMED
Basic UDI-DI
4981046-CFA2202-ZV EUDAMED
EMDN Code
Z1203020302 NON–INVASIVE BLOOD PRESSURE MONITORING INSTRUMENTS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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-Lars2m1kec 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

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

Manufacturer

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

Sources (1)

  • EUDAMED 74eb8039-6d9c-47fd-9937-d03d4759c44e 61 fields · synced Jun 17, 2026