Hemofilter Hollow Fiber Hemofilter (Acute Filter)
by Allmed Middle East 5 variants
Ref HH 80Model HH 2 HH 8 HH 10 HH 30 HH 40 HH 60 HH 80
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 | Number6221166HEMOFILTERREX | Date9 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- Withdrawn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
- Hemofilter Hollow Fiber Hemofilter (Acute Filter)Hollow Fiber Hemofilter “Acute Filter
- Model / Reference
- HH 2 HH 8 HH 10 HH 30 HH 40 HH 60 HH 80, HH 80
- Primary DI / UDI-DI
- 06221166010106, 06221166010151
- Basic UDI-DI
- 6221166HEMOFILTERREX, 6221166HemofilterEOEH
- Direct Marketing DI
- 0622116601010606221166010151
- EMDN Code
- F01060303 DIALYSERS - UFC > 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