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Tm-Cf302d

EUDAMED

Class I (EU MDR)

Ref TM-CF302D

by A&D Company, Limited

Identity

Device Name
TM-CF302D EUDAMED
Model / Reference
TM-CF302D EUDAMED

Identifiers

Primary DI / UDI-DI
05060006582462 EUDAMED
Basic UDI-DI
4981046-CFA2462-3C 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

Tm-Cf302d 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 9fff5dc6-6e4d-45f5-86fb-dee1b89bb200 61 fields · synced Jul 19, 2026