Skip to content

MediSet® Perfusion

by Paul Hartmann AG 20 variants

Ref 478739Model 3497

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number40495003497LJ Basic UDI-DI 04052199776163UDI-DIDate11 Jun 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
3497, 478739
Primary DI / UDI-DI
04052199776163
Basic UDI-DI
40495003497LJ
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class III
Medical Purpose
The injection/infusion sets are designed to realize an infusion or an injection by an access way (venous, central, subcutaneous).

Manufacturer details

EUDAMED SRN
DE-PR-000019925

Related devices

Category: Device sterilization/disinfection container, reusable

Other devices from Paul Hartmann AG

See all devices from Paul Hartmann AG →

Properties

  • Sterile