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IMMULITEยฎ / IMMULITE 1000 Insulin Sample Diluent - SFDA Registration ME0000001481SFDAA00719

Access comprehensive regulatory information for IMMULITEยฎ / 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.

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General IVD(Others)
ME0000001481SFDAA00719
IMMULITEยฎ / IMMULITE 1000 Insulin Sample Diluent
SFDA Registration: ME0000001481SFDAA00719
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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
Model Information
Model ID(s)
LINZ
Product Accessories

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