Saudi Arabia SFDA registration ME0000001503SFDAA01302
ImmunoCAP IgE/ECP/Tryptase Sample Diluent
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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About this record
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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