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RevoDx Mycoplasma Hominis/Genitalium qPCR Kit

EUDAMED

Class IVD General (EU MDR)

Ref IP202305-500

by İdi̇l Bi̇otech Araştirma San. Ve Ti̇c. Ltd. Şti̇.

Identity

Trade Name
RevoDx Mycoplasma Hominis/Genitalium qPCR Kit EUDAMED
Device Name
RevoDx Mycoplasma Hominis/Genitalium qPCR Kit EUDAMED
Model / Reference
IP202305-500 EUDAMED

Identifiers

Primary DI / UDI-DI
08684387212359 EUDAMED
Basic UDI-DI
B-08684387212359 EUDAMED
EMDN Code
W0105070501 STIS / STDS (C.TRACHOMATIS, N.GONORRHOEAE ,M.GENITALIUM, T.VAGINALIS, UREAPLASMA SPP….) COMBINATION - MULTIPLEX NA REAGENTS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

RevoDx Mycoplasma Hominis/Genitalium qPCR Kit by İdi̇l Bi̇otech Araştirma San. Ve Ti̇c. Ltd. Şti̇. — Class IVD General — IVDD — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
TR-MF-000047330

Sources (1)

  • EUDAMED 3a84ff61-c088-4b45-8b96-ec50f9129304 61 fields · synced Oct 6, 2026