Pure Global

Access Progesterone II Sample Diluent - SFDA Registration ME0000008377SFDAA00624

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.

Free Database
Powered by Pure Global AI
SFDA Official Data
2
ME0000008377SFDAA00624
Access Progesterone II Sample Diluent
SFDA Registration: ME0000008377SFDAA00624
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product 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

[]