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Mycoplasma Pneumoniae Antigen Rapid Qualitative Test

EUDAMED

Class IVD General (EU MDR)

Ref BT0102601

by Xiamen Biotime Biotechnology Co., Ltd.

Identity

Trade Name
Mycoplasma Pneumoniae Antigen Rapid Qualitative Test EUDAMED
Device Name
Mycoplasma Pneumoniae Antigen Rapid Qualitative Test EUDAMED
Model / Reference
BT0102601 EUDAMED

Identifiers

Primary DI / UDI-DI
06933260207985 EUDAMED
Basic UDI-DI
B-06933260207985 EUDAMED
EMDN Code
W0105010801 MYCOPLASMA ANTIGEN DETECTION EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Netherlands 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

No

EUDAMED

Surgical Instrument

No

EUDAMED

Mycoplasma Pneumoniae Antigen Rapid Qualitative Test by Xiamen Biotime Biotechnology 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-000012852
Authorised Representative
Medunion S.L. ES-AR-000019366

Sources (2)

  • EUDAMED f14dc1d5-d72c-49a7-b938-642dbc9926be 61 fields · synced Oct 6, 2026
  • EUDAMED f3f40f67-17c2-4ca9-a655-b2415e61934a 61 fields · synced Jul 14, 2026