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Saudi Arabia SFDA registration ME0000012833SFDAA00002Active

Radio Frequency Plasma Surgical System

Saudi ArabiaMDJIANGSU BONSS MEDICAL TECHNOLOGY CO., LTD.Class IIb
VerifiedSFDA · official registry
Product information

radiofrequency plasma electrosurgical

Product use

Indicated for cutting, excision, ablation, coagulation and hemostasis of soft tissues in surgical procedures. Usually, it is applicable for but not limited to ENT, Spinal, Orthopedics, Arthroscopic and Urology procedures, such as tonsillectomy, meniscectomy, lateral release, benign prostate hyperplasia, nucleoplasty, etc.

Device classification
Risk Class
Class IIb
Product Category
MD
Product Type
MD
Registration information
Registration ID
ME0000012833SFDAA00002
Authorization ID
GHTF-2019-6178
Status
Active
Expire Date
July 14, 2023
Manufacturer
Model information
ARS600 ARS700 ARS800 ARS900
Product accessories

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About this record

Access comprehensive regulatory information for Radio Frequency Plasma Surgical System 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 ME0000012833SFDAA00002 and manufactured by JIANGSU BONSS MEDICAL TECHNOLOGY CO., LTD..

This page provides complete registration details including product category (MD), 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.