Saudi Arabia SFDA registration ME0000001481SFDAA00839
IMMULITE 2000® Systems SUBS X2
Product information
Light emission which reacts with enzyme bound to the bead and is detected by a photomultiplier tube.
Product use
For use in the routine operation of the IMMULITE 2000 and IMMULITE 2500 Analyzers, as described in the Operator's Manuals.
Device classification
- Risk Class
- General IVD(Others)
- Product Category
- Chemicals
- Product Type
- IVD
Registration information
- Registration ID
- ME0000001481SFDAA00839
- Authorization ID
- GHTF-2019-2273
- Status
- Active
- Expire Date
- March 29, 2020
Manufacturer
- Manufacturer Name
- Siemens Healthcare diagnostics products Limited
Model information
- Model ID(s)
- L2SUBM
Product accessories
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About this record
Access comprehensive regulatory information for IMMULITE 2000® Systems SUBS X2 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 ME0000001481SFDAA00839 and manufactured by Siemens Healthcare diagnostics products Limited.
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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