Saudi Arabia SFDA registration ML0000000093SFDAA00013
KIMGUARD ONE-STEP KC500
Saudi Arabia·Medical Device·Arabian Medical Products Manufacturing Co., (ENAYAH)·Class IActiveProduct information
Sterilization Wrap
Product use
It is intended to allow sterilization of the enclosed medical device(s) and also to maintain sterility of the enclosed device(s) until opened.
Device classification
- Risk Class
- Class I
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ML0000000093SFDAA00013
- Authorization ID
- GHTF-2019-3483
- Status
- Active
- Expire Date
- February 06, 2022
Manufacturer
- Manufacturer Name
- Arabian Medical Products Manufacturing Co., (ENAYAH)
Model information
- Model ID(s)
- 62112 62115 62118 62120 62124 62130 62136 62140 62145 62147-C59 62148 62153-C61 62154 62172 62160
Product accessories
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About this record
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.
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