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Aquaflush® 200 Transanal Irrigation System – Standard Starter Set – Procedure Pack

by Clinisupplies (Nanjing) Co., Ltd.

Ref SPAF2-EU

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5060463890000PPVC0T5 Basic UDI-DI 05060458871282UDI-DIDate6 Jul 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  • Withdrawn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
Aquaflush® Transanal irrigation system – Procedure pack
Model / Reference
SPAF2-EU
Primary DI / UDI-DI
05060458871282
Basic UDI-DI
5060463890000PPVC0T5
EMDN Code
G99 Gastrointestinal devices - other
Device Class
Class I
Medical Purpose
The intended use of the product is for transanal irrigation of the bowel in adults and children 3 years and above with a bowel dysfunction, who have been assessed and trained by an appropriate healthcare professional.

Manufacturer details

EUDAMED SRN
CN-PR-000056275

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Properties

Other properties (1)

  • Sterile: No