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Hisense

EUDAMED

Class IIa (EU MDR)

Ref HD88ProModel HD 20 series to HD 60 series,HD 80 series,H7 and Aisense series

by Qingdao Hisense Medical Co., Ltd.

Identity

Trade Name
Hisense EUDAMED
Device Name
Ultrasound diagnostic systems HD 20 series to HD 60 series,Ultrasound diagnostic systems HD 80 series,Ultrasound diagnostic systems H7 and Aisense series EUDAMED
Model / Reference
HD 20 series to HD 60 series,HD 80 series,H7 and Aisense series EUDAMED
HD88Pro EUDAMED

Identifiers

Primary DI / UDI-DI
06978311951530 EUDAMED
Basic UDI-DI
697831195Ultrasound9F EUDAMED
EMDN Code
Z11040101 INTERNAL ULTRASOUND SCANNERS 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

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Hisense by Qingdao Hisense Medical Co., Ltd. — Class IIa — 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
CN-MF-000047224
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 5d427a84-5a71-4e79-b863-3086d7f33691 61 fields · synced Oct 5, 2026