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Lipotrol HDL/LDL Abnormal

EUDAMED

Class B (EU MDR)

Ref 981907

by Thermo Fisher Scientific Oy

Identity

Trade Name
Lipotrol HDL/LDL Abnormal EUDAMED
Device Name
Lipotrol HDL/LDL Abnormal EUDAMED
Model / Reference
981907 EUDAMED

Identifiers

Primary DI / UDI-DI
16438153819070 EUDAMED
Basic UDI-DI
6438153BU00142BN EUDAMED
Direct Marketing DI
16438153819070 EUDAMED
EMDN Code
W0101050202 LIPID CONTROLS EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

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

Lipotrol HDL/LDL Abnormal by Thermo Fisher Scientific Oy — 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

EUDAMED SRN
FI-MF-000001479

Sources (1)

  • EUDAMED d9efee42-2823-45ec-ad78-72fc0171d894 61 fields · synced Oct 6, 2026