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Fofo

by Foshan Hongfeng Co. Ltd. 25 variants

Ref FO3002GModel FO3002H,FO3002G

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69710664230000V3 Basic UDI-DI Date30 Jul 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Air compression therapy system
Hand recovery system
Model / Reference
FO3002G, FO3002H
Primary DI / UDI-DI
6971066422140, 06971066424120
Basic UDI-DI
69710664230000V3, 697106642HRSRB
EMDN Code
Z120607, Y241899
Device Class
Class IIa
Class I
EU market of registration
Denmark
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000016042
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Other devices from Foshan Hongfeng Co., Ltd.

See all devices from Foshan Hongfeng Co., Ltd. →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No