Evoke® Patient Controller (EPC)
Ref 1040
Evoke® Patient Controller (EPC) (1040) is a Class III device made by Saluda Medical Pty Ltd, registered in EUDAMED on 7 May 2024 (Basic UDI-DI 935230701040AU) with CE/MDR certificate MDR 776672 valid until 8 Apr 2029, active as of 25 Oct 2026.
Active
CE MDR
Valid until
8 Apr 2029
FDA recalls
Not applicable
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | NumberMDR 776672 | Date4 Sep 2026 | StatusActive |
Official records
- EUDAMED public site 935230701040AU
Certificates
- MDR 776672 Active
Technical documentation EU MDR
- Certifier
- BSI Group The Netherlands B.V. 2797
- Issued
- 4 Sep 2026
- Expires
- 8 Apr 2029
- Reason
- Other
Timeline
- Registered EUDAMED 935230701040AU
- Certificate issued EUDAMED MDR 776672
- Certificate expires EUDAMED MDR 776672
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / reference
- 1040
- Primary DI / UDI-DI
- 09352307001411
- Basic UDI-DI
- 935230701040AU
- EMDN code
- J020280 Spinal implantable neurostimulators - accessories
- Device class
- Class III
- EU registration type
- Standard device
- EU market of registration
- Netherlands
Manufacturer details
- EUDAMED SRN
- AU-MF-000010522
- Authorised representative
- MedR-AR Services B.V. NL-AR-000000120
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