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F47609

by FIAB S.p.A.

Ref F47609Model Peel-Away percutaneous introduction set

F47609 is a Class IIa device made by FIAB S.p.A., registered in EUDAMED on 12 May 2026 (Basic UDI-DI 803300326222000001MF), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number803300326222000001MF Basic UDI-DI 08033695724632UDI-DIDate12 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
Peel-Away percutaneous introduction set, F47609
Primary DI / UDI-DI
08033695724632
Basic UDI-DI
803300326222000001MF
EMDN code
C0503 Cardiovascular introducer sheaths, peel-away
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000005988

Similar devices in this category

Other devices filed under CARDIOVASCULAR INTRODUCER SHEATHS, PEEL-AWAY.

Other devices from FIAB S.p.A.

See all devices from FIAB S.p.A. →

Properties

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