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Vibrio Parahemolyticus Nucleic Acid Detection Kit(Isothermal Amplification)

EUDAMED

Class IVD General (EU MDR)

Ref F01004A-96Ref F01004A-24

by Jiangsu Qitian Gene biotechnology Co., Ltd

Identity

Device Name
Vibrio Parahemolyticus Nucleic Acid Detection Kit(Isothermal Amplification) EUDAMED
Model / Reference
F01004A-96 EUDAMED
F01004A-24 EUDAMED

Identifiers

Primary DI / UDI-DI
06975102440754 EUDAMED
06975102440778 EUDAMED
Basic UDI-DI
B-06975102440754 EUDAMED
B-06975102440778 EUDAMED
EMDN Code
W0105900102 REAGENTS FOR DNA AND/OR RNA AMPLIFICATION AND/OR DETECTION: BACTERIA AND/OR VIRUS 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

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

Vibrio Parahemolyticus Nucleic Acid Detection Kit(Isothermal Amplification) by Jiangsu Qitian Gene biotechnology Co., Ltd — Class IVD General — IVDD — listed…

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000050877
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (2)

  • EUDAMED 005b5114-761a-476f-b8fe-b8643599c707 61 fields · synced Jul 28, 2026
  • EUDAMED fa4d7b4d-29e2-442d-a6e5-2a2ec60f4db4 61 fields · synced May 18, 2026