← Back to catalogue

Verilab GMag

EUDAMED

Class A (EU MDR)

Ref LVE-0012Model 0012

by SIA Laboveritas

Identity

Trade Name
Verilab GMag EUDAMED
Device Name
VeriLab GMag EUDAMED
Model / Reference
0012 EUDAMED
LVE-0012 EUDAMED

Identifiers

Primary DI / UDI-DI
04751042630286 EUDAMED
Basic UDI-DI
4751042630012V4 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
Latvia EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

Verilab GMag by SIA Laboveritas — 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
SIA Laboveritas
EUDAMED SRN
LV-MF-000018225

Sources (1)

  • EUDAMED 860f9be0-5bcd-4caf-9f8f-fad1ae5024b4 61 fields · synced Jul 9, 2026