XERF EFFECTOR 40(300) Single box
by Cynosure Lutronic Technology Corporation
Ref XERF EFFECTOR 40(300) Single boxModel XERF EFFECTOR 40(300), XERF EFFECTOR 40(600), XERF EFFECTOR 40(900), XERF EFFECTOR 60(600), XERF EFFECTOR 60(900), XERF EFFECTOR 60(1200)
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 | Number88002918211011BGX 08800291821665 | Date22 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- Withdrawn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
- Electrosurgical electrode
- Model / Reference
- XERF EFFECTOR 40(300), XERF EFFECTOR 40(600), XERF EFFECTOR 40(900), XERF EFFECTOR 60(600), XERF EFFECTOR 60(900), XERF EFFECTOR 60(1200), XERF EFFECTOR 40(300) Single box
- Primary DI / UDI-DI
- 08800291821665
- Basic UDI-DI
- 88002918211011BGX
- EMDN Code
- X0599 High intensity electromagnetic radiation emitting equipment without an intended medical purpose intended for use on the human body, for skin resurfacing, tattoo or hair removal or other skin treatment – other
- Device Class
- Class IIb
- Market of Registration
- Netherlands
Manufacturer details
- EUDAMED SRN
- KR-MF-000047499
- Authorised representative
- Emergo Europe B.V. NL-AR-000000116
Other devices from Cynosure Lutronic Technology Corporation
See all devices from Cynosure Lutronic Technology Corporation →
Properties
Other properties (13)
- Sterile: No
- 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