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HUM PREC CONTROL 2 - SFDA Registration ME0000002169SFDAA00320

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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Annex II List B
ME0000002169SFDAA00320
HUM PREC CONTROL 2
SFDA Registration: ME0000002169SFDAA00320
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Product 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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