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m2000sp Instrument E-Series - SFDA Registration ME0000002992SFDAA00152

Access comprehensive regulatory information for m2000sp Instrument E-Series in the Saudi Arabia medical device market through Pure Global AI's free database. This Class II device is registered with Saudi Arabia SFDA under registration number ME0000002992SFDAA00152 and manufactured by Abbott Molecular Inc..

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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Class II
ME0000002992SFDAA00152
m2000sp Instrument E-Series
SFDA Registration: ME0000002992SFDAA00152
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Product Information

Fully automated sample preparation system

Product Use

the m2000sp fully automates the extraction of nucleic acid from the specimen and performance PCR plate preparation.

Device Classification
Risk Class
Class II
Product Category
Chemicals
Product Type
IVD
Registration Information
Registration ID
ME0000002992SFDAA00152
Authorization ID
GHTF-2019-1646
Status
Active
Expire Date
May 16, 2022
Manufacturer
Manufacturer Name
Abbott Molecular Inc.
Model Information
Model ID(s)
09K14-02
Product Accessories

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