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Single Use Preloaded Sphincterotome V - SFDA Registration ME0000002522SFDAA00174

Access comprehensive regulatory information for Single Use Preloaded 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 ME0000002522SFDAA00174 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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SFDA Official Data
Class IIb
ME0000002522SFDAA00174
Single Use Preloaded Sphincterotome V
SFDA Registration: ME0000002522SFDAA00174
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Product 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
ME0000002522SFDAA00174
Authorization ID
MDMA-1-2019-1577
Status
Active
Expire Date
May 26, 2024
Manufacturer
Model Information
Model ID(s)
KD-VC611Q-07201A // KD-VC611Q-07201S // KD-VC611Q-07203A // KD-VC611Q-07203S // KD-VC611Q-07301A // KD-VC611Q-07301S // KD-VC611Q-07303A // KD-VC611Q-07303S // KD-VC631Q-07201A // KD-VC631Q-07201S // KD-VC631Q-07203A // KD-VC631Q-07203S // KD-VC631Q-07301A // KD-VC631Q-07301S // KD-VC631Q-07303A // KD-VC631Q-07303S
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