Saudi Arabia SFDA registration ME0000002023SFDAA00592
UNIQO 160
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
- Manufacturer Name
- EUROIMMUN Medizinische Labordiagnostika AG
Model information
- Model ID(s)
- YG 2900-0101
Product accessories
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About this record
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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