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17-OH Progesterone Chemiluminescence Immunoassay Kit

EUDAMED

Class IVD General (EU MDR)

Ref 215E90001Model Reagents (include Calibrator and Control): 100tests/kit

by Nanjing RealMind Biotech Co., Ltd.

Identity

Device Name
17-OH Progesterone Chemiluminescence Immunoassay Kit EUDAMED
Model / Reference
Reagents (include Calibrator and Control): 100tests/kit EUDAMED
215E90001 EUDAMED

Identifiers

Primary DI / UDI-DI
06972719601301 EUDAMED
Basic UDI-DI
B-06972719601301 EUDAMED
EMDN Code
W0102050107 17 OH PROGESTERONE EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Hungary 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

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

17-OH Progesterone Chemiluminescence Immunoassay Kit by Nanjing RealMind 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-000024838
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED afe8c0a1-33c6-4b01-8613-358ea67c0c86 61 fields · synced Oct 6, 2026