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Fofo

EUDAMED

Class IIa (EU MDR)

Ref BC68001-E

by Foshan Hongfeng Co. Ltd.

Identity

Trade Name
FOFO EUDAMED
Device Name
Nebulizer EUDAMED
Model / Reference
BC68001-E EUDAMED

Identifiers

Primary DI / UDI-DI
6971066420696 EUDAMED
Basic UDI-DI
69710664268001-EN4 EUDAMED
EMDN Code
R060203 INHALATION THERAPY HUMIDIFICATION LIQUIDS 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

Fofo by Foshan Hongfeng 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-000016042
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 7be58e35-fdf0-4888-97e6-52224dc15164 61 fields · synced May 22, 2026