Saudi Arabia SFDA registration ML0000000093SFDAA00009
KIMGUARD 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
- ML0000000093SFDAA00009
- 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)
- 68112 68115 68118 68120 68124 68130 68136 68140 68145 68176 68148 68151-C 68160-01 68154 68172 68190 68160 68165
Product accessories
[]
About this record
Access comprehensive regulatory information for KIMGUARD 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 ML0000000093SFDAA00009 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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