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PurePrep Pathogen DGX

EUDAMED

Class A (EU MDR)

Ref OE00380960Ref OE0038025K

by magtivio B.V.

Identity

Trade Name
PurePrep Pathogen DGX EUDAMED
Device Name
MagSi-DX Pathogen EUDAMED
Model / Reference
OE00380960 EUDAMED
OE0038025K EUDAMED

Identifiers

Primary DI / UDI-DI
04260350320067 EUDAMED
04260350320081 EUDAMED
Basic UDI-DI
426035032DX0001PG 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
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

New Device

No

EUDAMED

Category: Nucleic acid extraction/isolation kit IVD

PurePrep Pathogen DGX by magtivio B.V. — 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

Manufacturer
magtivio B.V.
EUDAMED SRN
NL-MF-000023114

Sources (2)

  • EUDAMED 2cf49fd8-1822-42b2-84b2-a184269b33fa 61 fields · synced Aug 1, 2026
  • EUDAMED 6638d5f4-c0d3-4895-9bdb-412c238c38b3 61 fields · synced May 17, 2026