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nelaton catheter, for female

by Changzhou Huankang Medical Device Co., Ltd.

Ref HK-C02-12-F single bag

Active European Union

CE MDD

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06945934606321 Basic UDI-DI 06945934606321UDI-DIDate4 Aug 2026RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Model / Reference
HK-C02-12-F single bag
Primary DI / UDI-DI
06945934606321
Basic UDI-DI
B-06945934606321
EMDN Code
U01010502 Nelaton catheters, non self-lubricating
Device Class
Class I
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
CN-MF-000009030
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Changzhou Huankang Medical Device Co., Ltd.

See all devices from Changzhou Huankang Medical Device Co., Ltd. →

Properties

  • Sterile

Other properties (10)

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