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ImmunoCAP IgE/ECP/Tryptase Sample Diluent - SFDA Registration ME0000001503SFDAA01302

Access comprehensive regulatory information for ImmunoCAP IgE/ECP/Tryptase Sample Diluent 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 ME0000001503SFDAA01302 and manufactured by Phadia AB.

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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General IVD(Others)
ME0000001503SFDAA01302
ImmunoCAP IgE/ECP/Tryptase Sample Diluent
SFDA Registration: ME0000001503SFDAA01302
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Product Information

Reagents for use in ImmunoCAP instuments

Product Use

used for sample dilution in ImmunoCAP IgE/ECP/Tryptase tests

Device Classification
Risk Class
General IVD(Others)
Product Category
Chemicals
Product Type
IVD
Registration Information
Registration ID
ME0000001503SFDAA01302
Authorization ID
MDMA-1-2019-0390
Status
Active
Expire Date
February 17, 2025
Manufacturer
Manufacturer Name
Phadia AB
Model Information
Model ID(s)
10-9256-01, 10-9360-01
Product Accessories

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