Saudi Arabia SFDA registration ME0000015872SFDAA00980
Cystine Tellurite Agar Base
Product information
For selective isolation and differentiation of Corynebacterium diphtheriae types.
Device classification
- Risk Class
- 1
- Product Category
- IVD
- Product Type
- 2
Registration information
- Registration ID
- ME0000015872SFDAA00980
- 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)
- M881
Product accessories
[]
About this record
Access comprehensive regulatory information for Cystine Tellurite Agar Base 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 ME0000015872SFDAA00980 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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