Electrolase 7-100-12CS
Ref 7-100-12CS
Electrolase 7-100-12CS is a device classified as Class IIb in the EU and Class II in the US made by Conmed Corporation, registered in EUDAMED on 17 Jun 2026 (Basic UDI-DI B-30653405031646) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 30653405031646), active as of 24 Oct 2026.
Active
CE MDD
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-30653405031646 30653405031646 | Date17 Jun 2026 | StatusActive |
| United States | GUDID listing GUDID | Number30653405031646 | Date24 Sep 2016 | StatusListed |
Official records
- EUDAMED public site B-30653405031646
- AccessGUDID record 30653405031646
Across registries
- EUDAMED Basic UDI-DI B-30653405031646 registered 17 Jun 2026 Active
- FDA GUDID UDI-DI 30653405031646 listed 24 Sep 2016 Listed
Timeline
- Listed FDA GUDID 30653405031646
- Registered EUDAMED B-30653405031646
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Electrolase
- Generic name
- Open-surgery electrosurgical electrode, monopolar, single-use
- Device name
- Non-orthopedic, Active, Instrument, Electrosurgical, Electrode, Hyfrecator, Disposable
- Model / Ref / Catalog
- 7-100-12CS
- Primary DI / UDI-DI
- 30653405031646
- Basic UDI-DI
- B-30653405031646
- FDA product code
- GEI
- EMDN code
- K02030101 Radiofrequency surgery electrodes, single-use
- GMDN term
- Open-surgery electrosurgical electrode, monopolar, single-use
- Device class
- Class IIb EUDAMEDClass II GUDID
- Regulation number
- 878.4400
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Belgium
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class IIb | Class II |
| Implantable | Yes | No |
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