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Miyacath

EUDAMED

Class IIa (EU MDR)

Ref MYFA-WA 2014Model MIYACATH Antibacterial Hydrophilic Urinary Catheter -Ready To Use Female 20 CM 14 CH 30pcs/box

by İstem Medikal Tıbbi Cihaz ve Sanayi Ticaret Anonim Şirketi

Identity

Trade Name
MIYACATH EUDAMED
Device Name
MIYACATH Antibacterial Hydrophilic Urinary Catheter -Ready To Use Female 20 CM 14 CH EUDAMED
Model / Reference
MIYACATH Antibacterial Hydrophilic Urinary Catheter -Ready To Use Female 20 CM 14 CH 30pcs/box EUDAMED
MYFA-WA 2014 EUDAMED

Identifiers

Primary DI / UDI-DI
18699415735165 EUDAMED
Basic UDI-DI
B-18699415735165 EUDAMED
EMDN Code
U01010501 NELATON CATHETERS, SELF-LUBRICATING EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Intermittent urethral drainage catheter, non-antimicrobial, single-use

Miyacath by İstem Medikal Tıbbi Cihaz ve Sanayi Ticaret Anonim Şirketi — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Intermittent urethral drainage catheter, non-antimicrobial, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
TR-MF-000017811

Sources (1)

  • EUDAMED a4e53e63-435c-4985-8c0d-1f8372a784bc 61 fields · synced Jul 17, 2026