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PowerPrep™ Pathogen NA Extraction Kit EXP

EUDAMED

Class A (EU MDR)

Ref E0019Model E0019, E0019S

by KogeneBiotech Co., Ltd.

Identity

Trade Name
PowerPrep™ Pathogen NA Extraction Kit EXP EUDAMED
Device Name
PowerPrep™ Pathogen NA Extraction Kit EXP EUDAMED
Model / Reference
E0019, E0019S EUDAMED
E0019 EUDAMED

Identifiers

Primary DI / UDI-DI
08800056300060 EUDAMED
Basic UDI-DI
88000563E00195H EUDAMED
EMDN Code
W0105900101 REAGENTS FOR DNA AND/OR RNA EXTRACTION AND PREPARATION: BACTERIA AND/OR VIRUS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Czechia 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

New Device

No

EUDAMED

Category: Nucleic acid extraction/isolation kit IVD

PowerPrep™ Pathogen NA Extraction Kit EXP by KogeneBiotech 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-000045858
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (2)

  • EUDAMED 2ef2c3c0-ff32-4689-9d60-0a9940bda98f 61 fields · synced Jun 19, 2026
  • EUDAMED 31472316-617b-40be-8038-7408f1478ab5 61 fields · synced Jun 19, 2026