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Neisseria Gonorrhoeae Detection Kit (Fluorescence PCR)

EUDAMED

Class IVD General (EU MDR)

Ref ANG01-AOG48E;,ANG01-AOG96E,ANG01D-AOG48E, ANG01D-AOG96E

by Zhejiang Orient Gene Biotech Co., Ltd

Identity

Device Name
Neisseria Gonorrhoeae Detection Kit (Fluorescence PCR) EUDAMED
Model / Reference
ANG01-AOG48E;,ANG01-AOG96E,ANG01D-AOG48E, ANG01D-AOG96E EUDAMED

Identifiers

Primary DI / UDI-DI
D-69509960ANG01QDQJ EUDAMED
Basic UDI-DI
B-69509960ANG01QDQJ EUDAMED
EMDN Code
W0105010203 GONOCOCCAL DETECTION BY NA REAGENTS 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

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 Detection Kit (Fluorescence PCR) by Zhejiang Orient Gene Biotech Co., Ltd — 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-000017965
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (2)

  • EUDAMED 60a03379-0220-44be-b8f8-268b6cce65c7-1 61 fields · synced Jul 30, 2026
  • EUDAMED 60a03379-0220-44be-b8f8-268b6cce65c7-2 61 fields · synced Jul 30, 2026