Saudi Arabia SFDA registration ME0000002119SFDAA00149ActiveEnhanced Bipolar Forceps
The endoscopic instruments intended for endoscopic manipulation for tissue
- Risk Class
- 3
- Product Category
- Medical Device
- Product Type
- 1
- Registration ID
- ME0000002119SFDAA00149
- Authorization ID
- MDMA-2-2024-3477
- Status
- Active
- Expire Date
- December 06, 2027
- Manufacturer Name
- Shenzhen Edge Medical Co., Ltd.
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Access comprehensive regulatory information for Enhanced Bipolar Forceps in the Saudi Arabia medical device market through Pure Global AI's free database. This 3 device is registered with Saudi Arabia SFDA under registration number ME0000002119SFDAA00149 and manufactured by Shenzhen Edge Medical Co., Ltd. .
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.