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SINGLE USE INJECTOR - SFDA Registration ME0000002522SFDAA00163

Access comprehensive regulatory information for SINGLE USE INJECTOR in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIa device is registered with Saudi Arabia SFDA under registration number ME0000002522SFDAA00163 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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SFDA Official Data
Class IIa
ME0000002522SFDAA00163
SINGLE USE INJECTOR
SFDA Registration: ME0000002522SFDAA00163
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Product Information

NON ACTIVE INSTRUMENTS USED IN CONJUNCTION WITH ENDOSCOPES

Product Use

This instrument has been designed to be used with an Olympus endoscope to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract.

Device Classification
Risk Class
Class IIa
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000002522SFDAA00163
Authorization ID
GHTF-2018-1031
Status
Active
Expire Date
November 02, 2022
Manufacturer
Model Information
Model ID(s)
NM-400L-0423//NM-400L-0621//NM-400L-0425//NM-400L-0523//NM-400L-0525//NM-400L-0623//NM-400L-0625//NM-400U-0323//NM-400U-0423//NM-400U-0425//NM-400U-0523//NM-400U-0525//NM-400U-0623//NM-400U-0625//NM-400Y-0423//NM-401L-0623//NM-401L-0423 //NM-401L-0425//NM-401L-0523//NM-401L-0525 //NM-401L-0625//NM-400L-0421
Product Accessories

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