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ImmunoCAP Gliadin IgA/IgG Control L - SFDA Registration ME0000001503SFDAA01343

Access comprehensive regulatory information for ImmunoCAP Gliadin IgA/IgG Control L 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 ME0000001503SFDAA01343 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)
ME0000001503SFDAA01343
ImmunoCAP Gliadin IgA/IgG Control L
SFDA Registration: ME0000001503SFDAA01343
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Product Information

IVD test kit for the quantitative measurement of IgA and IgG antibodies specific for gliadin

Product Use

in vitro diagnostic use as an aid in the clinical diagnosis of patients with celiac disease and dermatitis herpetiformis

Device Classification
Risk Class
General IVD(Others)
Product Category
Chemicals
Product Type
IVD
Registration Information
Registration ID
ME0000001503SFDAA01343
Authorization ID
GHTF-2016-2483
Status
Active
Expire Date
October 16, 2019
Manufacturer
Manufacturer Name
Phadia AB
Model Information
Model ID(s)
10-9484-03
Product Accessories

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