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LyoSens Haemophilus Ducreyi Detection qPCR Kit

EUDAMED

Class IVD General (EU MDR)

Ref LYO81

by Vitrosens Biotechnology Inc.

Identity

Trade Name
LyoSens Haemophilus Ducreyi Detection qPCR Kit EUDAMED
Device Name
Haemophilus Ducreyi Detection qPCR Kit EUDAMED
Model / Reference
LYO81 EUDAMED

Identifiers

Primary DI / UDI-DI
08684595034958 EUDAMED
Basic UDI-DI
B-08684595034958 EUDAMED
EMDN Code
W0105900102 REAGENTS FOR DNA AND/OR RNA AMPLIFICATION AND/OR DETECTION: BACTERIA AND/OR VIRUS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany 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

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

Yes

EUDAMED

Surgical Instrument

Yes

EUDAMED

LyoSens Haemophilus Ducreyi Detection qPCR Kit by Vitrosens Biotechnology Inc. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
TR-MF-000026452

Sources (1)

  • EUDAMED 65ee4623-9021-4475-b1db-f91b5110a736 61 fields · synced Aug 3, 2026