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V80 eluent C

EUDAMED

Class A (EU MDR)

Ref 0320200914Model 600 mL

by Shenzhen Lifotronic Technology Co., Ltd.

Identity

Device Name
V80 eluent C EUDAMED
Model / Reference
600 mL EUDAMED
0320200914 EUDAMED

Identifiers

Primary DI / UDI-DI
06975984062754 EUDAMED
Basic UDI-DI
69703416803202036HT EUDAMED
EMDN Code
W0201050201 HIGH PERFORMANCE LIQUID CHROMATOGRAPHY SYSTEMS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Italy 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

V80 eluent C by Shenzhen Lifotronic Technology Co., Ltd. — 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

EUDAMED SRN
CN-MF-000005654
Authorised Representative
Umedwings Netherlands B.V. NL-AR-000000444

Sources (1)

  • EUDAMED ba8b6e3d-e6b0-49ff-adf5-50f6b4c66e50 61 fields · synced Jun 18, 2026