DistricAth Ti 135 P1, 7
by Districlass Medical SA 11 variants
Ref KP4021765, KP4021736, KP4021737, KP4021744, KP4021725, KP4021757, KP4021714, D4021762, KP4021742, KP4021724, KP4021749
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- Withdrawn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
- Device Name
- DistricAth Ti
- Model / Reference
- KP4021765, KP4021736, KP4021737, KP4021744, KP4021725, KP4021757, KP4021714, D4021762, KP4021742, KP4021724, KP4021749
- Primary DI / UDI-DI
- 03665642035307, 03665642035079, 03665642035086, 03665642035154, 03665642034973, 03665642035246, 03665642013435, 03665642010915, 03665642035130, 03665642034966, 03665642035192
- 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