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Fofo

EUDAMED

Class I (EU MDR)

Ref HF6101Model HF6100,HF6101

by Foshan Hongfeng Co. Ltd.

Identity

Trade Name
FOFO EUDAMED
Device Name
Water bed EUDAMED
Model / Reference
HF6100,HF6101 EUDAMED
HF6101 EUDAMED

Identifiers

Primary DI / UDI-DI
06971066423918 EUDAMED
Basic UDI-DI
697106642WB61HJ EUDAMED
EMDN Code
V080702 NON ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

Yes

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 I — 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 c29e6377-fc54-4074-b0fc-99bcb3c3e5fd 61 fields · synced May 22, 2026