Saudi Arabia SFDA registration ML0000000093SFDAA00008
KIMGUARD KC200
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
- ML0000000093SFDAA00008
- 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)
- 68205 68202 68203 68204 68201 68012 68014 68014-C18 68015 68018 68020 68024 68025 68025-C36 68026-C48 68030 68036 68039-C 68040-CR 68040 68045 68048 68054-C 68072-01 68051-C 68053-CR 68054 68072 68055 68059-CR 68060
Product accessories
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About this record
Access comprehensive regulatory information for KIMGUARD KC200 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 ML0000000093SFDAA00008 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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