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Buffer

EUDAMED

Class A (EU MDR)

Ref 0320501904Model 480 mL, 6×480 mL, 2×2 L, 2×1 L, 4×1 L, 4×2 L

by Shenzhen Lifotronic Technology Co., Ltd.

Identity

Trade Name
Buffer EUDAMED
Device Name
Buffer EUDAMED
Model / Reference
480 mL, 6×480 mL, 2×2 L, 2×1 L, 4×1 L, 4×2 L EUDAMED
0320501904 EUDAMED

Identifiers

Primary DI / UDI-DI
06970341689513 EUDAMED
Basic UDI-DI
69703416803205065JP EUDAMED
EMDN Code
W01029003 BUFFERS (UNASSIGNABLE), SUPPLEM. REAGENTS, ETC (IC) 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

Buffer 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 568e230b-9dc0-4ad7-84c5-c68ec63a8abe 61 fields · synced Jun 18, 2026