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Flexor® Tuohy-Borst Side-Arm Introducer Shuttle Select® - SFDA Registration ME0000006512SFDAA01496

Access comprehensive regulatory information for Flexor® Tuohy-Borst Side-Arm Introducer Shuttle Select® in the Saudi Arabia medical device market through Pure Global AI's free database. This 4 device is registered with Saudi Arabia SFDA under registration number ME0000006512SFDAA01496 and manufactured by Cook Incorporated.

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.

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ME0000006512SFDAA01496
Flexor® Tuohy-Borst Side-Arm Introducer Shuttle Select®
SFDA Registration: ME0000006512SFDAA01496
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Product Information

Flexor shaft with a hemostasis valve and are provided with one or more dilators

Device Classification
Risk Class
4
Product Category
Medical Device
Product Type
1
Registration Information
Registration ID
ME0000006512SFDAA01496
Authorization ID
MDMA-2-2025-0329
Status
Active
Expire Date
January 27, 2028
Manufacturer
Manufacturer Name
Cook Incorporated
Model Information
Model ID(s)
KSAW-5.0-38-90-RB-SHTL-FLEX-HC,KSAW-6.0-38-90-RB-SHTL-FLEX-HC
Product Accessories

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