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Single Use Biliary Drainage Stent V - SFDA Registration ME0000002522SFDAA00158

Access comprehensive regulatory information for Single Use Biliary Drainage Stent V 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 ME0000002522SFDAA00158 and manufactured by Olympus Medical Systems Corp..

This page provides complete registration details including product category (MD), 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
ME0000002522SFDAA00158
Single Use Biliary Drainage Stent V
SFDA Registration: ME0000002522SFDAA00158
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Product Information

Endotherapy Devices

Product Use

This instrument has been designed to be used with Olympus endoscopes for endoscopic retrograde biliary drainage (ERBD).

Device Classification
Risk Class
Class IIb
Product Category
MD
Product Type
MD
Registration Information
Registration ID
ME0000002522SFDAA00158
Authorization ID
GHTF-2018-1058
Status
Active
Expire Date
November 02, 2022
Manufacturer
Model Information
Model ID(s)
PBD-V631P-1215 // PBD-V632P-0705 // PBD-V632P-0707 // PBD-V632P-0709 // PBD-V632P-0712 // PBD-V632P-0715 // PBD-V632P-0805 // PBD-V632P-0807 // PBD-V632P-0809 // PBD-V632P-0812 // PBD-V632P-0815 // PBD-V632P-1005 // PBD-V632P-1007 // PBD-V632P-1009 // PBD-V632P-1012 // PBD-V632P-1015 // PBD-V632P-1205 // PBD-V632P-1207 // PBD-V632P-1209 // PBD-V632P-1212 // PBD-V632P-1215
Product Accessories

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