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Neofuser Twin

by S&S Med Co., Ltd. 72 variants

Ref G30-T

Neofuser Twin (G30-T) is a Class IIb device made by S&S Med Co., Ltd., registered in EUDAMED on 12 Aug 2025 (Basic UDI-DI B-08800331530076), active as of 24 Oct 2026.

Active European Union

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08800331530076 Basic UDI-DI 08800331530076UDI-DIDate12 Aug 2025RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Single Use Infusion Pump
Model / reference
G30-T
Primary DI / UDI-DI
08800331530076
Basic UDI-DI
B-08800331530076
EMDN code
A05010101 Elastomeric systems - fixed flow w/o additional bolus
Device class
Class IIb
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
KR-MF-000017308
Authorised representative
Easy Medical Device CommV BE-AR-000011902

Similar devices in this category

Other devices filed under ELASTOMERIC SYSTEMS - FIXED FLOW W/O ADDITIONAL BOLUS.

Other devices from S&S Med Co., Ltd.

See all devices from S&S Med Co., Ltd. →

Properties

  • Supplied sterile
  • Sterilise before use
  • Administering medicine
Other properties (9, all answered No)