Saudi Arabia SFDA registration ME0000015872SFDAA00967
Staphylococcus Agar No.110 (Gelatin Mannitol Salt Agar)
Saudi Arabia·IVD·HIMEDIA LABORATORIES PVT LTD·1ActiveProduct 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
- Manufacturer Name
- HIMEDIA LABORATORIES PVT LTD
Model information
- Model ID(s)
- M521
Product accessories
[]
About this record
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.
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