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NAxtra®

EUDAMED

Class A (EU MDR)

Ref LSNX5000

by Lybe Scientific AS

Identity

Trade Name
NAxtra® EUDAMED
Device Name
NAxtra® nucleic acid extraction kit EUDAMED
Model / Reference
LSNX5000 EUDAMED

Identifiers

Primary DI / UDI-DI
07090060540212 EUDAMED
Basic UDI-DI
709006054LSNXC5 EUDAMED
Direct Marketing DI
07090060540212 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
Norway 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

Yes

EUDAMED

Category: Nucleic acid extraction/isolation kit IVD

NAxtra® by Lybe Scientific AS — 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
Lybe Scientific AS
EUDAMED SRN
NO-MF-000023842

Sources (1)

  • EUDAMED 0c26775c-1856-418e-b86b-dc67c857e0e6 61 fields · synced Jul 19, 2026