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Verilab GVTM

EUDAMED

Class A (EU MDR)

Ref LVT-0017Model 0017

by SIA Laboveritas

Identity

Trade Name
Verilab GVTM EUDAMED
Device Name
VeriLab GVTM EUDAMED
Model / Reference
0017 EUDAMED
LVT-0017 EUDAMED

Identifiers

Primary DI / UDI-DI
04751042630040 EUDAMED
Basic UDI-DI
4751042630040V9 EUDAMED
EMDN Code
W0104010203 TRANSPORT MEDIA EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Latvia 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

Verilab GVTM by SIA Laboveritas — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
SIA Laboveritas
EUDAMED SRN
LV-MF-000018225

Sources (1)

  • EUDAMED 0e7c84a7-0c6c-454a-892a-cf7e6f9ea6de 61 fields · synced Jun 18, 2026