Saudi Arabia SFDA registration ME0000002522SFDAA00163
SINGLE USE INJECTOR
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
- Manufacturer Name
- Olympus Medical Systems Corp.
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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About this record
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.
Free DatabasePowered by Pure Global AISFDA Official DataClass IIa