DistricAth Ti 235 PM5 P2, 0
by Districlass Medical SA 13 variants
Ref KP1322012, KP1322014, KP1322041, KP1322026, KP1322042, KP1022012, KP1322064, KP1322044, KP1022025, KP1322037, KP1322030
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number3665642Art.22MDRTiCS | Date23 Oct 2025 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Trade Name
- DistricAth Ti 235 PM5 P2,0DistricAth Ti 235 P2,0
- Device Name
- DistricAth Ti
- Model / Reference
- KP1322012, KP1322014, KP1322041, KP1322026, KP1322042, KP1022012, KP1322064, KP1322044, KP1022025, KP1322037, KP1322030
- Primary DI / UDI-DI
- 03665642039053, 03665642014005, 03665642039282, 03665642039145, 03665642039299, 03665642033303, 03665642039459, 03665642039312, 03665642031712, 03665642039244, 03665642039183
- Basic UDI-DI
- 3665642Art.22MDRTiCS
- EMDN Code
- C01020401 Subcutaneous implantable venous access port systems, single-chamber
- Device Class
- Class III
- Medical Purpose
- Les chambres à cathéter implantables DistricAth® sont des dispositifs médicaux permettant un accès transcutané au système vasculaire intraveineux dans le cadre de traitements itératifs et de longue durée d’un patient : Chimiothérapie, antibiothérapie, nutrition parentérale, prélèvement ou injection de produits sanguins.
Manufacturer details
- EUDAMED SRN
- FR-PR-000009488