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Chromsystems Elution Buffer Levetiracetam (Keppraยฎ) in serum/plasma - SFDA Registration ME0000009057SFDAA00724

Access comprehensive regulatory information for Chromsystems Elution Buffer 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 ME0000009057SFDAA00724 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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ME0000009057SFDAA00724
Chromsystems Elution Buffer Levetiracetam (Keppraยฎ) in serum/plasma
SFDA Registration: ME0000009057SFDAA00724
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Product Information

Substance used to elute the analytes from solid phase extraction columns

Device Classification
Risk Class
1
Product Category
IVD
Product Type
2
Registration Information
Registration ID
ME0000009057SFDAA00724
Authorization ID
MDMA-2-2025-0487
Status
Active
Expire Date
February 14, 2028
Manufacturer
Model Information
Model ID(s)
24010
Product Accessories

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