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8900-005054-40

by FIAB S.p.A.

Ref 8900-005054-40Model Disposable electrodes defibrillation, cardioversion, cardiac stimulator, ECG

8900-005054-40 is a Class IIb device made by FIAB S.p.A., registered in EUDAMED on 30 Jan 2026 (Basic UDI-DI 803300326808000007U5), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number803300326808000007U5 Basic UDI-DI 08054751934536UDI-DIDate30 Jan 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
Disposable electrodes defibrillation, cardioversion, cardiac stimulator, ECG, 8900-005054-40
Primary DI / UDI-DI
08054751934536
Basic UDI-DI
803300326808000007U5
EMDN code
C020401 External cardioversion defibrillator electrode pads
Device class
Class IIb
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 EXTERNAL CARDIOVERSION DEFIBRILLATOR ELECTRODE PADS.

Other devices from FIAB S.p.A.

See all devices from FIAB S.p.A. →

Properties

Other properties (14, all answered No)