Saudi Arabia SFDA registration ME0000002202SFDAA00060
AirLife™ Reduced Heparin Arterial Blood Sampler
Product information
Blood Sampling Devices.
Product use
Arterial blood samplers for pH, Blood Gas, Electrolyte and Metabolite Analysis.
Device classification
- Risk Class
- Class IIa
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000002202SFDAA00060
- Authorization ID
- GHTF-2016-0644
- Status
- Active
- Expire Date
- November 02, 2019
Manufacturer
- Manufacturer Name
- CareFusion
Model information
- Model ID(s)
- 4022LRH 4023LRH 4023RH 9023RHSL 9025RH
Product accessories
[]
About this record
Access comprehensive regulatory information for AirLife™ Reduced Heparin Arterial Blood Sampler 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 ME0000002202SFDAA00060 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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