Saudi Arabia SFDA registration ME0000009057SFDAA00722
Chromsystems Wash Buffer 1 Levetiracetam (Keppra®) in serum/plasma
Saudi Arabia·IVD·Chromsystems Instruments&Chemicals GmbH·1ActiveProduct 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
- Manufacturer Name
- Chromsystems Instruments&Chemicals GmbH
Model information
- Model ID(s)
- 24007
Product accessories
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About this record
Access comprehensive regulatory information for Chromsystems Wash Buffer 1 Levetiracetam (Keppra®) 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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