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V60 eluent A

EUDAMED

Class A (EU MDR)

Ref 0320200901Model 1000 mL

by Shenzhen Lifotronic Technology Co., Ltd.

Identity

Device Name
V60 eluent A EUDAMED
Model / Reference
1000 mL EUDAMED
0320200901 EUDAMED

Identifiers

Primary DI / UDI-DI
06975984062693 EUDAMED
Basic UDI-DI
69703416803202030HF 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

V60 eluent A 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 642ebf75-55d7-48f2-b356-8809e340a0ca 61 fields · synced Jul 11, 2026