Ed Coil
by KANEKA Corporation 134 variants
Ref 353-0303R
Active
CE MDD
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD | NumberB-04540778142039 04540778142039 | Date25 Dec 2025 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
Specification
- Model / reference
- 353-0303R
- Primary DI / UDI-DI
- 04540778142039
- Basic UDI-DI
- B-04540778142039
- EMDN code
- C010402020301 Embolisation coils
- Device class
- Class III
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- JP-MF-000022143
- Authorised representative
- Kaneka Medical Europe N.V. BE-AR-000010091
Other devices from Kaneka Corp.
Properties
Other properties (12)
- Sterilise before use: No
- Reusable: No
- Contains latex: No
- Reprocessed single-use device: No
- Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
- Incorporates a substance derived from human blood or plasma: No
- Contains human tissues or cells: No
- Contains animal tissues or cells: No
- Contains endocrine-disrupting substances: No
- Administering medicine: No
- Measuring function: No
- Incorporates a medicinal substance: No