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UNIQO 160 - SFDA Registration ME0000002023SFDAA00592

Access comprehensive regulatory information for UNIQO 160 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 ME0000002023SFDAA00592 and manufactured by EUROIMMUN Medizinische Labordiagnostika AG.

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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1
ME0000002023SFDAA00592
UNIQO 160
SFDA Registration: ME0000002023SFDAA00592
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Product Information

for fully automated processing of indirect immunofluorescence tests (IIFT).

Device Classification
Risk Class
1
Product Category
IVD
Product Type
2
Registration Information
Registration ID
ME0000002023SFDAA00592
Authorization ID
MDMA-2-2024-3479
Status
Active
Expire Date
December 11, 2027
Manufacturer
Model Information
Model ID(s)
YG 2900-0101
Product Accessories

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