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StrongStep® Neisseria gonorrhoeae Antigen Rapid Test

EUDAMED

Class IVD General (EU MDR)

Ref 500020Model 20 Tests/box

by Nanjing Liming Bio-products Co. Ltd

Identity

Trade Name
StrongStep® Neisseria gonorrhoeae Antigen Rapid Test EUDAMED
Device Name
Neisseria gonorrhoeae Antigen Rapid Test EUDAMED
Model / Reference
20 Tests/box EUDAMED
500020 EUDAMED

Identifiers

Primary DI / UDI-DI
06973181850341 EUDAMED
Basic UDI-DI
B-06973181850341 EUDAMED
EMDN Code
W0105010201 GONOCOCCAL ANTIGEN DETECTION EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Northern Ireland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

StrongStep® Neisseria gonorrhoeae Antigen Rapid Test by Nanjing Liming Bio-products Co. Ltd — Class IVD General — IVDD — listed in EUDAMED

Manufacturer's product page: Neisseria gonorrhoeae/Chlamydia trachomatis/Mycoplasma genitalium Antigen Combo Rapid Test

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000041298
Authorised Representative
Wellkang Ltd XI-AR-000001836

Sources (1)

  • EUDAMED ebf293ea-55a5-486f-8ff1-41f302fec764 61 fields · synced Jun 19, 2026