Polyethersulfone Hollow Fiber Hemodialyzers (VAPORIA, VAPORIA HF)
by Allmed Middle East 14 variants
Ref VAPORIA 200Model VAPORIA 100 VAPORIA 130 VAPORIA 140 VAPORIA 160 VAPORIA 180 VAPORIA 200 VAPORIA 220
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 | Number6221166VAPSTHDYE 06221166012391 | Date13 Jun 2026 | 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- Withdrawn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
- Polyethersulfone Hollow Fiber Hemodialyzers (VAPORIA, VAPORIA HF)
- Model / Reference
- VAPORIA 100 VAPORIA 130 VAPORIA 140 VAPORIA 160 VAPORIA 180 VAPORIA 200 VAPORIA 220, VAPORIA 200
- Primary DI / UDI-DI
- 06221166012391
- Basic UDI-DI
- 6221166VAPSTHDYE
- Direct Marketing DI
- 06221166012391
- EMDN Code
- F01060203 DIALYSERS - UFC = 18 - 35 ml/h/mmHg, SYNTHETIC MEMBRANES
- Device Class
- Class IIb
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- EG-MF-000025747
- Authorised representative
- Allmed Medical GmbH DE-AR-000007830
Other devices from Allmed Middle East
Properties
Other properties (12)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No