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Rappaport Vassiliadis R10 Medium - SFDA Registration ME0000015872SFDAA00987

Access comprehensive regulatory information for Rappaport Vassiliadis R10 Medium 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 ME0000015872SFDAA00987 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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ME0000015872SFDAA00987
Rappaport Vassiliadis R10 Medium
SFDA Registration: ME0000015872SFDAA00987
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Product Information

For selectively enriching Salmonella species from meat and dairy products faeces and sewage polluted

Device Classification
Risk Class
1
Product Category
IVD
Product Type
2
Registration Information
Registration ID
ME0000015872SFDAA00987
Authorization ID
MDMA-2-2025-0042
Status
Active
Expire Date
January 04, 2028
Manufacturer
Model Information
Model ID(s)
M1530
Product Accessories

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