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Respiratory High-Flow Therapy Device

EUDAMED

Class IIa (EU MDR)

Ref H-80AS

by BMC Medical Co., Ltd.

Identity

Trade Name
Respiratory High-Flow Therapy Device EUDAMED
Device Name
Respiratory High-Flow Therapy Device EUDAMED
Model / Reference
H-80AS EUDAMED

Identifiers

Primary DI / UDI-DI
06948538369005 EUDAMED
Basic UDI-DI
69485383HF001PQ EUDAMED
Direct Marketing DI
06948538369005 EUDAMED
EMDN Code
R060202 OXYGEN ADMINISTRATION HUMIDIFICATION SYSTEMS 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

Respiratory High-Flow Therapy Device by BMC 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-000010157
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED dc272fc0-c998-4f84-b235-d8c979d033aa 61 fields · synced Jun 19, 2026