Saudi Arabia SFDA registration ME0000002522SFDAA00175
Single Use Sphincterotome V
Saudi Arabia·MD·Olympus Medical Systems Corp.·Class IIbActiveProduct information
Sphincterotome
Product use
These instruments (sphincterotomes and guidewires) have been designed to be used with an Olympus endoscope for papillotomy using high-frequency current.
Device classification
- Risk Class
- Class IIb
- Product Category
- MD
- Product Type
- MD
Registration information
- Registration ID
- ME0000002522SFDAA00175
- Authorization ID
- MDMA-1-2019-1577
- Status
- Active
- Expire Date
- May 26, 2024
Manufacturer
- Manufacturer Name
- Olympus Medical Systems Corp.
Model information
- Model ID(s)
- KD-VC431Q-0730 // KD-VC433Q-0720 // KD-VC433Q-0730
Product accessories
[]
About this record
Access comprehensive regulatory information for Single Use Sphincterotome 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 ME0000002522SFDAA00175 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