Saudi Arabia SFDA registration ME0000006512SFDAA01494
Flexor® Tuohy-Borst Side-Arm Introducer Shuttle® - SL
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
- ME0000006512SFDAA01494
- Authorization ID
- MDMA-2-2025-0329
- Status
- Active
- Expire Date
- January 27, 2028
Manufacturer
- Manufacturer Name
- Cook Incorporated
Model information
- Model ID(s)
- KSAW-4.0-18/35-110-RB-SHTL-HC,KSAW-4.0-18/35-90-RB-SHTL-HC,KSAW-5.0-18/38-110-RB-SHTL-HC,KSAW-5.0-18/38-90-RB-SHTL,KSAW-5.0-18/38-90-RB-SHTL-HC,KSAW-6.0-38-110-RB-SHTL-HC,KSAW-6.0-38-80-RB-SHTL,KSAW-6.0-38-80-RB-SHTL-HC,KSAW-6.0-38-90-RB-SHTL,KSAW-6.0-38-90-RB-SHTL-HC,KSAW-7.0-38-80-RB-SHTL,KSAW-7.0-38-80-RB-SHTL-HC,KSAW-7.0-38-90-RB-SHTL,KSAW-7.0-38-90-RB-SHTL-HC,KSAW-8.0-38-80-RB-SHTL-HC,KSAW-8.0-38-90-RB-SHTL-HC
Product accessories
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About this record
Access comprehensive regulatory information for Flexor® Tuohy-Borst Side-Arm Introducer Shuttle® - SL 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 ME0000006512SFDAA01494 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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