Saudi Arabia SFDA registration ME0000001503SFDAA01321
ImmunoCAP Allergen w82, Careless weed
Saudi Arabia·Chemicals·Phadia AB·General IVD(Others)ActiveProduct information
Lab test for the determination of allergen Specific IgE in human serum or plasma
Product use
In Vitro quantitative measurement of allergen Specific IgE in human serum or plasma. It is intented for In Vitro Diagnostic use as an aid in the clinical diagnosis of IgE mediated allergic disorders in conjunction with other clinical findings
Device classification
- Risk Class
- General IVD(Others)
- Product Category
- Chemicals
- Product Type
- IVD
Registration information
- Registration ID
- ME0000001503SFDAA01321
- Authorization ID
- MDMA-1-2019-0388
- Status
- Active
- Expire Date
- February 10, 2025
Manufacturer
- Manufacturer Name
- Phadia AB
Model information
- Model ID(s)
- 14-4953-01
Product accessories
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About this record
Access comprehensive regulatory information for ImmunoCAP Allergen w82, Careless weed 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 ME0000001503SFDAA01321 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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