← Back to catalogue

MagSi-DX Pathogen

EUDAMED

Class A (EU MDR)

Ref MDDX0001025K

by magtivio B.V.

Identity

Trade Name
MagSi-DX Pathogen EUDAMED
Device Name
MagSi-DX Pathogen EUDAMED
Model / Reference
MDDX0001025K EUDAMED

Identifiers

Primary DI / UDI-DI
04260350320043 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

MagSi-DX Pathogen 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 89a60469-0ed5-4288-90ed-dabea76db55d 61 fields · synced Jun 18, 2026