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Chromsystems Wash Buffer 1 Levetiracetam (Keppraยฎ) in serum/plasma - SFDA Registration ME0000009057SFDAA00722

Access comprehensive regulatory information for Chromsystems Wash Buffer 1 Levetiracetam (Keppraยฎ) in serum/plasma in the Saudi Arabia medical device market through Pure Global AI's free database. This 1 device is registered with Saudi Arabia SFDA under registration number ME0000009057SFDAA00722 and manufactured by Chromsystems Instruments&Chemicals GmbH.

This page provides complete registration details including product category (IVD), 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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1
ME0000009057SFDAA00722
Chromsystems Wash Buffer 1 Levetiracetam (Keppraยฎ) in serum/plasma
SFDA Registration: ME0000009057SFDAA00722
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Product Information

First solvent used to flush the solid phase extraction columns

Device Classification
Risk Class
1
Product Category
IVD
Product Type
2
Registration Information
Registration ID
ME0000009057SFDAA00722
Authorization ID
MDMA-2-2025-0487
Status
Active
Expire Date
February 14, 2028
Manufacturer
Model Information
Model ID(s)
24007
Product Accessories

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