Saudi Arabia SFDA registration ME0000002202SFDAA00055
AirLife® Meconium Suction Device (Kurtis MSD)
Saudi Arabia·Medical Device·CareFusion·Class IIaActiveProduct information
Tracheal Suction Catheter.
Product use
The MSD (Meconium Suction Device) is indicated for the suctioning of meconium secretions from the oropharynx and trachea of newborn infants. It can be easily adapted to allow endotracheal positive pressure ventilation during resuscitation.
Device classification
- Risk Class
- Class IIa
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000002202SFDAA00055
- Authorization ID
- GHTF-2016-0642
- Status
- Active
- Expire Date
- November 02, 2019
Manufacturer
- Manufacturer Name
- CareFusion
Model information
- Model ID(s)
- 4530VS 4535EU
Product accessories
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About this record
Access comprehensive regulatory information for AirLife® Meconium Suction Device (Kurtis MSD) in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIa device is registered with Saudi Arabia SFDA under registration number ME0000002202SFDAA00055 and manufactured by CareFusion.
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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