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Neisseria Gonorrhoeae DNA Fluorescence Diagnostic Kit (PCR-Fluorescence Probing)

EUDAMED

Class IVD General (EU MDR)

Ref S3003E

by Sansure Biotech Inc.

Identity

Trade Name
Neisseria Gonorrhoeae DNA Fluorescence Diagnostic Kit (PCR-Fluorescence Probing) EUDAMED
Device Name
Neisseria Gonorrhoeae DNA Fluorescence Diagnostic Kit (PCR-Fluorescence Probing) EUDAMED
Model / Reference
S3003E EUDAMED

Identifiers

Primary DI / UDI-DI
06955792730786 EUDAMED
06955792730793 EUDAMED
Basic UDI-DI
B-06955792730786 EUDAMED
B-06955792730793 EUDAMED
EMDN Code
W0105010203 GONOCOCCAL DETECTION BY NA REAGENTS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

Yes

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

Neisseria Gonorrhoeae DNA Fluorescence Diagnostic Kit (PCR-Fluorescence Probing) by Sansure Biotech Inc. — 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
CN-MF-000011392
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (2)

  • EUDAMED 65610152-382b-43d3-846c-995ced1ee45a 61 fields · synced Jul 21, 2026
  • EUDAMED d7912df6-502c-48bd-ae25-20f4e6df366b 61 fields · synced May 19, 2026