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Eluent B

EUDAMED

Class A (EU MDR)

Ref 0320200503Model 400 mL, 800 mLRef 0320202803

by Shenzhen Lifotronic Technology Co., Ltd.

Identity

Trade Name
Eluent B EUDAMED
Device Name
Eluent B EUDAMED
Model / Reference
400 mL, 800 mL EUDAMED
0320200503 EUDAMED
0320202803 EUDAMED

Identifiers

Primary DI / UDI-DI
06975984060415 EUDAMED
06975984066219 EUDAMED
Basic UDI-DI
69703416803202039HZ EUDAMED
69703416803202043HQ EUDAMED
EMDN Code
W0103010299 OTHER HAEMOGLOBIN (TYPES) TESTING - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Netherlands 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

Eluent B 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 (2)

  • EUDAMED 8e2f0dc6-5928-488d-94c8-9096668df34f 61 fields · synced Jul 21, 2026
  • EUDAMED 081a5c57-5e84-49df-9dc4-5f03480f82e8 61 fields · synced May 18, 2026