Saudi Arabia SFDA registration ME0000001481SFDAA00838
IMMULITE®/IMMULITE® 1000 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 with the IMMULITE and IMMULITE 1000 Systems. Follow instructions in the IMMULITE or IMMULITE 1000 Operator's Manual.
Device classification
- Risk Class
- General IVD(Others)
- Product Category
- Chemicals
- Product Type
- IVD
Registration information
- Registration ID
- ME0000001481SFDAA00838
- 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)
- LSUBX
Product accessories
[]
About this record
Access comprehensive regulatory information for IMMULITE®/IMMULITE® 1000 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 ME0000001481SFDAA00838 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.
Free DatabasePowered by Pure Global AISFDA Official DataGeneral IVD(Others)