Saudi Arabia SFDA registration ME0000002522SFDAA00158
Single Use Biliary Drainage Stent V
Saudi Arabia·MD·Olympus Medical Systems Corp.·Class IIbActiveProduct 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
- Manufacturer Name
- Olympus Medical Systems Corp.
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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About this record
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.
Free DatabasePowered by Pure Global AISFDA Official DataClass IIb