KIMGUARD ONE-STEP KC500 - SFDA Registration ML0000000093SFDAA00013
Access comprehensive regulatory information for KIMGUARD ONE-STEP KC500 in the Saudi Arabia medical device market through Pure Global AI's free database. This Class I device is registered with Saudi Arabia SFDA under registration number ML0000000093SFDAA00013 and manufactured by Arabian Medical Products Manufacturing Co., (ENAYAH).
This page provides complete registration details including product category (Medical Device), 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.
Sterilization Wrap
It is intended to allow sterilization of the enclosed medical device(s) and also to maintain sterility of the enclosed device(s) until opened.
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