Saudi Arabia SFDA registration ME0000002169SFDAA00320
HUM PREC CONTROL 2
Saudi Arabia·Chemicals·Randox Laboratories Ltd.·Annex II List BActiveProduct information
UNASSAYED SERUM
Product use
This product is intended for in vitro diagnostic use as an unassayed control to monitor laboratory precision on clinical chemistry
systems.
Device classification
- Risk Class
- Annex II List B
- Product Category
- Chemicals
- Product Type
- IVD
Registration information
- Registration ID
- ME0000002169SFDAA00320
- Authorization ID
- GHTF-2017-0694
- Status
- Active
- Expire Date
- November 18, 2023
Manufacturer
- Manufacturer Name
- Randox Laboratories Ltd.
Model information
- Model ID(s)
- UN1557
Product accessories
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About this record
Access comprehensive regulatory information for HUM PREC CONTROL 2 in the Saudi Arabia medical device market through Pure Global AI's free database. This Annex II List B device is registered with Saudi Arabia SFDA under registration number ME0000002169SFDAA00320 and manufactured by Randox Laboratories Ltd..
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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