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latex foley catheter

by Ningbo Pinmed Instruments Co., Ltd. 7 variants

Ref GTFL230_12

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06970879339256 Basic UDI-DI 06970879339256UDI-DIDate21 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  • Withdrawn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

Device Name
urethral catheter
Model / Reference
GTFL230_12
Primary DI / UDI-DI
06970879339256
Basic UDI-DI
B-06970879339256
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
  • Contains Latex

Other properties (9)

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