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Miyacath

by İstem Medikal Tıbbi Cihaz ve Sanayi Ticaret Anonim Şirketi 143 variants

Ref MYFA 2018Model MIYACATH Antibacterial Hydrophilic Urinary Catheter Female 20 CM 18 CH 40pcs/box

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-18699415702037 Basic UDI-DI 18699415702037UDI-DIDate25 May 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  • Withdrawn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
MIYACATH Antibacterial Hydrophilic Urinary Catheter Female 20 CM 18 CH
Model / Reference
MIYACATH Antibacterial Hydrophilic Urinary Catheter Female 20 CM 18 CH 40pcs/box, MYFA 2018
Primary DI / UDI-DI
18699415702037
Basic UDI-DI
B-18699415702037
EMDN Code
U01010501 Nelaton catheters, self-lubricating
Device Class
Class IIa
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000017811

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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