Saudi Arabia SFDA registration ME0000001481SFDAA00719
IMMULITE® / IMMULITE 1000 Insulin Sample Diluent
Product information
Diluent for the insulin assay
Product use
For the manual dilution of samples. One vial with 25 mL of ready-to-use, insulin-free nonhuman serum matrix, with preservative.
Device classification
- Risk Class
- General IVD(Others)
- Product Category
- Chemicals
- Product Type
- IVD
Registration information
- Registration ID
- ME0000001481SFDAA00719
- Authorization ID
- MDMA-1-2019-2267
- Status
- Active
- Expire Date
- May 27, 2025
Manufacturer
- Manufacturer Name
- Siemens Healthcare Diagnostics Products Limited
Model information
- Model ID(s)
- LINZ
Product accessories
[]
About this record
Access comprehensive regulatory information for IMMULITE® / IMMULITE 1000 Insulin Sample Diluent 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 ME0000001481SFDAA00719 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)