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P PLATE - SFDA Registration ME0000002522SFDAA00176

Access comprehensive regulatory information for P PLATE 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 ME0000002522SFDAA00176 and manufactured by Olympus Medical Systems Corp..

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.

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Class IIb
ME0000002522SFDAA00176
P PLATE
SFDA Registration: ME0000002522SFDAA00176
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Product Information

Electrosurgical Equipment Disposable Patient Plate

Product Use

This electrosurgical unit has been designed to be used with an Olympus endoscope (fiberscope or videoscope) compatible with electrosurgery, light source, electrosurgical accessories and other ancillary equipment for general and endoscopic electrosurgery (cutting and coagulation).

Device Classification
Risk Class
Class IIb
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000002522SFDAA00176
Authorization ID
GHTF-2017-0838
Status
Active
Expire Date
November 02, 2022
Manufacturer
Model Information
Model ID(s)
MAJ-897
Product Accessories

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