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Supercath Clampcath

by Togo Medikit Co., Ltd. 5 variants

Ref SP502-17(33)

Supercath Clampcath (SP502-17(33)) is a Class IIa device made by Togo Medikit Co., Ltd., registered in EUDAMED on 9 Jul 2026 (Basic UDI-DI 4543527Clampcath_EA), active as of 24 Oct 2026.

Active European Union

CE MDR

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/MDR Number4543527Clampcath_EA Basic UDI-DI 04543527000772UDI-DIDate9 Jul 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
SP502-17(33)
Primary DI / UDI-DI
04543527000772
Basic UDI-DI
4543527Clampcath_EA
EMDN code
A010401 Arteriovenous fistula needles
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Germany

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 ARTERIOVENOUS FISTULA NEEDLES.

Other devices from Togo Medikit Co., Ltd.

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

Properties

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