Skip to content

Rayflow

by Hexacath

Ref RFW6

Rayflow (RFW6) is a Class IIb device made by Hexacath, registered in EUDAMED on 28 Jul 2026 (Basic UDI-DI B-03700385765781), 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-03700385765781 Basic UDI-DI 03700385765781UDI-DIDate28 Jul 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
RFW6
Primary DI / UDI-DI
03700385765781
Basic UDI-DI
B-03700385765781
EMDN code
C0104010203 Pharmaceutical infusion and administration intracoronary and intracardiac catheters
Device class
Class IIb
EU registration type
Legacy device (under a directive)
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000010342

Similar devices in this category

Other devices filed under CORONARY ANGIOGRAPHY THERAPEUTIC DEVICES.

Other devices from Hexacath

See all devices from Hexacath →

Properties

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