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EUROBlotMaster - SFDA Registration ME0000002023SFDAA00002

Access comprehensive regulatory information for EUROBlotMaster in the Saudi Arabia medical device market through Pure Global AI's free database. This General IVD(Others) device is registered with Saudi Arabia SFDA under registration number ME0000002023SFDAA00002 and manufactured by EUROIMMUN Medizinische Labordiagnostika AG.

This page provides complete registration details including product category (Chemicals), 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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SFDA Official Data
General IVD(Others)
ME0000002023SFDAA00002
EUROBlotMaster
SFDA Registration: ME0000002023SFDAA00002
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Product Information

washing and incubation device for up to 30 strips for the processing of biological samples

Product Use

diagnostics of autoimmune and infectious diseases or allergies.

Device Classification
Risk Class
General IVD(Others)
Product Category
Chemicals
Product Type
IVD
Registration Information
Registration ID
ME0000002023SFDAA00002
Authorization ID
GHTF-2016-0503
Status
Active
Expire Date
March 01, 2019
Manufacturer
Model Information
Model ID(s)
YG 0151-0101
Product Accessories

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