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Hecht verwijder set

by STS Medical Group EAD 2 variants

Ref 29554-04

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number380023TD06URIIQM Basic UDI-DI 03800232429009UDI-DIDate23 Jun 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  • Withdrawn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

Model / Reference
29554-04
Primary DI / UDI-DI
03800232429009
Basic UDI-DI
380023TD06URIIQM
EMDN Code
V0502 Clinical administration kits not included in other classes
Device Class
Class I
Medical Purpose
Disposable procedure pack, combination of devices for disease alleviation related to urinary catheterization.

Manufacturer details

EUDAMED SRN
BG-PR-000041814

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Properties

Other properties (1)

  • Sterile: No