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Air Mattress

by Foshan Duson Medical Technology Co., Ltd.

Ref DS8001Model DS8001,DS8002,DS8003,DS8004,DS8005,DS8006,DS8007,DS8008,DS8009,DS8010

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, self-declared

Class I: no certifier involved

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 Number697792826AM01R2 Basic UDI-DI 06977928266136UDI-DIDate28 Apr 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Air Mattress
Model / Reference
DS8001, DS8002, DS8003, DS8004, DS8005, DS8006, DS8007, DS8008, DS8009, DS8010
Primary DI / UDI-DI
06977928266136
Basic UDI-DI
697792826AM01R2
EMDN Code
V08068002 Bed supports
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000044392
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Foshan Duson Medical Technology Co., Ltd.

See all devices from Foshan Duson Medical Technology 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