Saudi Arabia SFDA registration ME0000008377SFDAA00622
ACCESS PROGESTERONE II
Product information
Chemiluminescent immunoassay for the quantitative determination of progesterone in human serum
Device classification
- Risk Class
- 2
- Product Category
- IVD
- Product Type
- 2
Registration information
- Registration ID
- ME0000008377SFDAA00622
- Authorization ID
- MDMA-2-2025-0266
- Status
- Active
- Expire Date
- January 22, 2028
Manufacturer
- Manufacturer Name
- Beckman Coulter Inc.
Model information
- Model ID(s)
- C78020
Product accessories
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About this record
Access comprehensive regulatory information for ACCESS PROGESTERONE II in the Saudi Arabia medical device market through Pure Global AI's free database. This 2 device is registered with Saudi Arabia SFDA under registration number ME0000008377SFDAA00622 and manufactured by Beckman Coulter Inc..
This page provides complete registration details including product category (IVD), 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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