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Profilis PaincAth

by Districlass Medical SA 16 variants

Ref P500-07.5QR

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3665642Art22MDRPaincAth43 Basic UDI-DI 03665642300771UDI-DIDate23 Oct 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  • Withdrawn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

Device Name
PaincAth
Model / Reference
P500-07.5QR
Primary DI / UDI-DI
03665642300771
Basic UDI-DI
3665642Art22MDRPaincAth43
EMDN Code
A030499 Administration kits - other
Device Class
Class IIb
Medical Purpose
Les cathéters multiperforés Profilis PaincAth® sont des dispositifs médicaux permettant la diffusion in situ de médicaments analgésiques de manière continue et homogène au niveau d’une plaie opératoire suite à un acte chirurgical.

Manufacturer details

EUDAMED SRN
FR-PR-000009488

Other devices from Districlass Medical SA

See all devices from Districlass Medical SA →

Properties

  • Sterile