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silicone foley catheter

by Ningbo Pinmed Instruments Co., Ltd. 10 variants

Ref GTFS230_20

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-06970879339386 Basic UDI-DI 06970879339386UDI-DIDate30 Jun 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  • Withdrawn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
GTFS230_20
Primary DI / UDI-DI
06970879339386
Basic UDI-DI
B-06970879339386
EMDN Code
U010299 Urethral prostatic and bladder catheters, with balloon - other
Device Class
Class IIa
Market of Registration
Lithuania

Manufacturer details

EUDAMED SRN
CN-MF-000008488
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from Ningbo Pinmed Instruments Co., Ltd.

See all devices from Ningbo Pinmed Instruments 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