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Tryptose Agar - SFDA Registration ME0000015872SFDAA00969

Access comprehensive regulatory information for Tryptose 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 ME0000015872SFDAA00969 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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ME0000015872SFDAA00969
Tryptose Agar
SFDA Registration: ME0000015872SFDAA00969
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Product Information

For isolation, cultivation and differentiation primarily of Brucella and other pathogenic microorgan

Device Classification
Risk Class
1
Product Category
IVD
Product Type
2
Registration Information
Registration ID
ME0000015872SFDAA00969
Authorization ID
MDMA-2-2025-0042
Status
Active
Expire Date
January 04, 2028
Manufacturer
Model Information
Model ID(s)
M538
Product Accessories

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