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Ecstasy 1000 Calibrator - SFDA Registration ME0000002950SFDAA00002

Access comprehensive regulatory information for Ecstasy 1000 Calibrator 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 ME0000002950SFDAA00002 and manufactured by Microgenics Corporation.

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)
ME0000002950SFDAA00002
Ecstasy 1000 Calibrator
SFDA Registration: ME0000002950SFDAA00002
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Product Information

Calibrators for Ecstasy

Product Use

The MULTIGENT Ecstasy Calibrators are intended for the calibration of the MULTIGENT Ecstasy assay, which detects 3,4-methylenedioxymethamphetamine (MDMA) in human urine on the ARCHITECT c Systems

Device Classification
Risk Class
General IVD(Others)
Product Category
Chemicals
Product Type
IVD
Registration Information
Registration ID
ME0000002950SFDAA00002
Authorization ID
GHTF-2019-2933
Status
Active
Expire Date
September 12, 2022
Manufacturer
Manufacturer Name
Microgenics Corporation
Model Information
Model ID(s)
3L42-04
Product Accessories

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