Highflex
by Angiomed GmbH & Co. Medizintechnik KG 21 variants
Ref 42252080
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 | Number0801741CIZEAGUSSA 00801741209963 | Date20 Oct 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- Withdrawn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
- Highflex™ Stone Basket
- Model / Reference
- 42252080
- Primary DI / UDI-DI
- 00801741209963
- Basic UDI-DI
- 0801741CIZEAGUSSA
- EMDN Code
- U090101 Urinary stone retrieval baskets
- Device Class
- Class I
- EU market of registration
- Belgium
Manufacturer details
- EUDAMED SRN
- DE-MF-000014844
Other devices from Angiomed GmbH & Co. Medizintechnik KG
See all devices from Angiomed GmbH & Co. Medizintechnik KG →
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