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Hemostasis Valve Sets

by SCW Medicath Ltd. 9 variants

Ref 42.03.10001

Hemostasis Valve Sets (42.03.10001) is a Class I device made by SCW Medicath Ltd., registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI B-06938820508533), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06938820508533 Basic UDI-DI 06938820508533UDI-DIDate29 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
42.03.10001
Primary DI / UDI-DI
06938820508533
Basic UDI-DI
B-06938820508533
EMDN code
C900101 Haemostasis valves
Device class
Class I
EU registration type
Legacy device (under a directive)
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
CN-MF-000019140
Authorised representative
Obelis s.a. BE-AR-000000106

Similar devices in this category

Other devices filed under HAEMOSTASIS VALVES.

Other devices from SCW Medicath Ltd.

See all devices from SCW Medicath Ltd. →

Properties

  • Supplied sterile
Other properties (11, all answered No)