Saudi Arabia SFDA registration ME0000005736SFDAA00189
SureFit™
Saudi Arabia·Medical Device·CONMED CORPORATION·Class IIbActiveProduct information
Dispersive electrodes
Product use
Designed for use with only those electrosurgical generators equipped with Contact Quality Monitoring (CQM) systems during electrosurgery and provides a path for RF energy produced at the active electrode to return to the generator.
Device classification
- Risk Class
- Class IIb
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000005736SFDAA00189
- Authorization ID
- MDMA-1-2019-3362
- Status
- Active
- Expire Date
- June 18, 2026
Manufacturer
- Manufacturer Name
- CONMED CORPORATION
Model information
- Model ID(s)
- 410-2000 410-2100 410-2200
Product accessories
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About this record
Access comprehensive regulatory information for SureFit™ in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIb device is registered with Saudi Arabia SFDA under registration number ME0000005736SFDAA00189 and manufactured by CONMED CORPORATION.
This page provides complete registration details including product category (Medical Device), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.
Free DatabasePowered by Pure Global AISFDA Official DataClass IIb