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Fofo

EUDAMED

Class IIa (EU MDR)

Ref FO3002

by Foshan Hongfeng Co. Ltd.

Identity

Trade Name
Fofo EUDAMED
Device Name
FO3002 EUDAMED
Model / Reference
FO3002 EUDAMED

Identifiers

Primary DI / UDI-DI
06971066420146 EUDAMED
Basic UDI-DI
697106642FO30027P EUDAMED
EMDN Code
V080701 ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

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 da6af8d6-fb58-4d62-b211-422066caa63b 61 fields · synced May 22, 2026