Saudi Arabia SFDA registration ME0000008377SFDAA00624
Access Progesterone II Sample Diluent
Saudi Arabia·IVD·Beckman Coulter Inc.·2ActiveProduct information
The Sample Diluent is intended to dilute samples containing progesterone
Device classification
- Risk Class
- 2
- Product Category
- IVD
- Product Type
- 2
Registration information
- Registration ID
- ME0000008377SFDAA00624
- Authorization ID
- MDMA-2-2025-0266
- Status
- Active
- Expire Date
- January 22, 2028
Manufacturer
- Manufacturer Name
- Beckman Coulter Inc.
Model information
- Model ID(s)
- C81798
Product accessories
[]
About this record
Access comprehensive regulatory information for Access Progesterone II Sample Diluent 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 ME0000008377SFDAA00624 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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