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Mast Isoplex® Vtec

EUDAMED

Class B (EU MDR)

Ref DNA/LYO3

by Mast Group Limited

Identity

Trade Name
MAST ISOPLEX® VTEC EUDAMED
Device Name
MAST ISOPLEX® VTEC EUDAMED
Model / Reference
DNA/LYO3 EUDAMED

Identifiers

Primary DI / UDI-DI
15056152705326 EUDAMED
Basic UDI-DI
50561527LYO3NL EUDAMED
Direct Marketing DI
15056152705326 EUDAMED
EMDN Code
W02050285 MICRO-ARRAY INSTRUMENTS - CONSUMABLES EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Germany 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

No

EUDAMED

Mast Isoplex® Vtec by Mast Group Limited — Class B — 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
Mast Group Limited
EUDAMED SRN
GB-MF-000025209
Authorised Representative
Mast Diagnostica GmbH DE-AR-000005299

Sources (1)

  • EUDAMED 0e52e9d0-2a69-4cd9-99a0-a1531a725827 61 fields · synced Jul 10, 2026