Saudi Arabia SFDA registration ME0000003930SFDAA00007ActiveFluorescence Endoscope
Provides high resolution imaging for realtime visible and near infrared fluorescence surgery
- Risk Class
- 2
- Product Category
- Medical Device
- Product Type
- 1
- Registration ID
- ME0000003930SFDAA00007
- Authorization ID
- MDMA-2-2025-0341
- Status
- Active
- Expire Date
- January 28, 2028
- Manufacturer Name
- Shenzhen Edge Medical Co., Ltd.
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Access comprehensive regulatory information for Fluorescence Endoscope in the Saudi Arabia medical device market through Pure Global AI's free database. This 2 device is registered with Saudi Arabia SFDA under registration number ME0000003930SFDAA00007 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.