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ACCESS PROGESTERONE II - SFDA Registration ME0000008377SFDAA00622

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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ME0000008377SFDAA00622
ACCESS PROGESTERONE II
SFDA Registration: ME0000008377SFDAA00622
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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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