DERIVO peripher Embolisation Device
by Acandis GmbH Germany EUDAMED
Ref 01-102510
EMDN P070402020102
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number426065033DERIVOperipherD9 | Date29 Apr 2026 | StatusActive |
Coverage
- Active
- Not covered
European Union — CE/MDR Active
Certificates
- 1000302304 Supplemented
Technical documentation EU MDR
- Notified body
- Notified body 0297
- Issued
- 16 Mar 2026
- Expires
- 10 Jul 2029
- Reason
- Change approved
- 1000331236 Supplemented
Quality management system EU MDR
- Notified body
- Notified body 0297
- Issued
- 6 Aug 2026
- Expires
- 22 Mar 2028
- Reason
- Change approved
Specification
- Model / Reference
- 01-102510
- Primary DI / UDI-DI
- 04260650334665
- Basic UDI-DI
- 426065033DERIVOperipherD9
- Direct Marketing DI
- 04260650334665
- EMDN Code
- P070402020102 Non-stainless steel peripheral vascular bare metal stents
- Device Class
- Class IIb
- Market of Registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000006259
Other devices from Acandis GmbH
Properties & raw data
Show properties, registry sources and raw records
Other properties (12)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Sutures: 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
Sources (1)
- EUDAMED 04260650334665|426065033DERIVOPERIPHERD9