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MediSet® Perfusion

by Laboratoires PAUL HARTMANN S.à.r.l 28 variants

Ref 478713Model 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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number32614834975T Basic UDI-DI 03261480002350UDI-DIDate26 Nov 2024RegisteredStatusActive

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  • Withdrawn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, 478713
Primary DI / UDI-DI
03261480002350
Basic UDI-DI
32614834975T
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
FR-PR-000004030

Related devices

Category: Device sterilization/disinfection container, reusable

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Properties

  • Sterile