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KIMGUARD ONE-STEP KC200 - SFDA Registration ML0000000093SFDAA00012

Access comprehensive regulatory information for KIMGUARD ONE-STEP 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 ML0000000093SFDAA00012 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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SFDA Official Data
Class I
ML0000000093SFDAA00012
KIMGUARD ONE-STEP KC200
SFDA Registration: ML0000000093SFDAA00012
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Product 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
ML0000000093SFDAA00012
Authorization ID
GHTF-2019-3483
Status
Active
Expire Date
February 06, 2022
Model Information
Model ID(s)
62012 62015 62018 62020 62024 62030 62036 62040 62045 62048 62060-02 62054 62072 62060 62060-01
Product Accessories

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