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Fp002

EUDAMED

Class A (EU MDR)

Ref FP002Model RADIPREP

by KH Medical Co., Ltd.

Identity

Model / Reference
RADIPREP EUDAMED
FP002 EUDAMED

Identifiers

Primary DI / UDI-DI
08800204300355 EUDAMED
Basic UDI-DI
88002043RADIPREPSD EUDAMED
EMDN Code
W0105900101 REAGENTS FOR DNA AND/OR RNA EXTRACTION AND PREPARATION: BACTERIA AND/OR VIRUS EUDAMED

Classification

Device Class
Class A EUDAMED
Special Device Type
Software EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Category: Nucleic acid extraction/isolation kit IVD

Fp002 by KH Medical Co., Ltd. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Nucleic acid extraction/isolation kit IVD.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
KR-MF-000017883
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (1)

  • EUDAMED 7af1c578-0028-438a-a09d-f1670771d777 61 fields · synced Jun 19, 2026