Pure Global

Staphylococcus Agar No.110 (Gelatin Mannitol Salt Agar) - SFDA Registration ME0000015872SFDAA00967

Access comprehensive regulatory information for Staphylococcus Agar No.110 (Gelatin Mannitol Salt Agar) in the Saudi Arabia medical device market through Pure Global AI's free database. This 1 device is registered with Saudi Arabia SFDA under registration number ME0000015872SFDAA00967 and manufactured by HIMEDIA LABORATORIES PVT LTD.

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
1
ME0000015872SFDAA00967
Staphylococcus Agar No.110 (Gelatin Mannitol Salt Agar)
SFDA Registration: ME0000015872SFDAA00967
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Information

Used as a selective medium for the isolation and testing of pathogenic Staphylococci.

Device Classification
Risk Class
1
Product Category
IVD
Product Type
2
Registration Information
Registration ID
ME0000015872SFDAA00967
Authorization ID
MDMA-2-2025-0042
Status
Active
Expire Date
January 04, 2028
Manufacturer
Model Information
Model ID(s)
M521
Product Accessories

[]