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Saudi Arabia SFDA registration ME0000002119SFDAA00154Active

Enhanced Forceps

Saudi ArabiaMedical DeviceShenzhen Edge Medical Co., Ltd. 3
VerifiedSFDA · official registry
Product information

The endoscopic instruments intended for endoscopic manipulation for tissue

Device classification
Risk Class
3
Product Category
Medical Device
Product Type
1
Registration information
Registration ID
ME0000002119SFDAA00154
Authorization ID
MDMA-2-2024-3477
Status
Active
Expire Date
December 06, 2027
Manufacturer
Manufacturer Name
Shenzhen Edge Medical Co., Ltd.
Model information
MP1318,MP4-PG-P
Product accessories

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About this record

Access comprehensive regulatory information for Enhanced 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 ME0000002119SFDAA00154 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.