← Back to catalogue

Fetal doppler

EUDAMED

Class IIa (EU MDR)

Ref AD51AModel AD50A

by Hunan Accurate Bio-Medical Technology Co., Ltd.

Identity

Trade Name
Fetal doppler EUDAMED
Device Name
Fetal doppler EUDAMED
Model / Reference
AD51A EUDAMED
AD50A EUDAMED

Identifiers

Primary DI / UDI-DI
06927394502016 EUDAMED
06927394588881 EUDAMED
Basic UDI-DI
B-06927394502016 EUDAMED
69273945FD01SD EUDAMED
Direct Marketing DI
06927394588881 EUDAMED
EMDN Code
Z12080103 FOETAL HEARTBEAT DETECTORS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Fetal doppler by Hunan Accurate Bio-Medical Technology Co., Ltd. — Class IIa — CE/MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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

Manufacturer

EUDAMED SRN
CN-MF-000012835
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (2)

  • EUDAMED caab0b04-3326-4208-9091-5d3ba0251c99 61 fields · synced Oct 7, 2026
  • EUDAMED 1feed769-7119-4b6b-9273-54c2a10ee3c0 61 fields · synced May 19, 2026