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VIDAS HIV DUO AG/AB - SFDA Registration ME0000001030SFDAA00910

Access comprehensive regulatory information for VIDAS HIV DUO AG/AB in the Saudi Arabia medical device market through Pure Global AI's free database. This 4 device is registered with Saudi Arabia SFDA under registration number ME0000001030SFDAA00910 and manufactured by BIOMERIEUX S.A..

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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ME0000001030SFDAA00910
VIDAS HIV DUO AG/AB
SFDA Registration: ME0000001030SFDAA00910
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Product Information

use for combined detection of anti-HIV-1,anti-HIV-2 and HIV-1 p24 in human serum or plasma

Device Classification
Risk Class
4
Product Category
IVD
Product Type
2
Registration Information
Registration ID
ME0000001030SFDAA00910
Authorization ID
MDMA-2-2025-0096
Status
Active
Expire Date
January 11, 2028
Manufacturer
Manufacturer Name
BIOMERIEUX S.A.
Model Information
Model ID(s)
424480
Product Accessories

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