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Supercath 5

by Togo Medikit Co., Ltd. 7 variants

Ref SP125-22-31T

Supercath 5 (SP125-22-31T) is a Class IIa device made by Togo Medikit Co., Ltd., registered in EUDAMED on 13 Aug 2026 (Basic UDI-DI B-04543527238878), 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-04543527238878 Basic UDI-DI 04543527238878UDI-DIDate13 Aug 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
SP125-22-31T
Primary DI / UDI-DI
04543527238878
Basic UDI-DI
B-04543527238878
EMDN code
C0101010202 Peripheral i.v. catheters, with safety systems, w/o injection valves
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
JP-MF-000013805
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Similar devices in this category

Other devices filed under PERIPHERAL I.V. CATHETERS, WITH SAFETY SYSTEMS.

Other devices from Togo Medikit Co., Ltd.

See all devices from Togo Medikit Co., Ltd. →

Properties

  • Supplied sterile
Other properties (13, all answered No)