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Neofuser Plus

EUDAMED

Class IIb (EU MDR)

Ref X2030E

by S&S Med Co., Ltd.

Identity

Trade Name
Neofuser Plus EUDAMED
Device Name
Single Use Infusion Pump EUDAMED
Model / Reference
X2030E EUDAMED

Identifiers

Primary DI / UDI-DI
08800027767670 EUDAMED
Basic UDI-DI
B-08800027767670 EUDAMED
EMDN Code
A05010102 ELASTOMERIC SYSTEMS - FIXED FLOW WITH ADDITIONAL BOLUS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Neofuser Plus by S&S Med Co., Ltd. — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
S&S Med Co., Ltd.
EUDAMED SRN
KR-MF-000017308
Authorised Representative
Easy Medical Device BE-AR-000011902

Sources (1)

  • EUDAMED 51151a0c-2763-4d86-b8f7-26fa026600d7 61 fields · synced Jun 18, 2026