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KIMGUARD KC100 - SFDA Registration ML0000000093SFDAA00007

Access comprehensive regulatory information for KIMGUARD KC100 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 ML0000000093SFDAA00007 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
ML0000000093SFDAA00007
KIMGUARD KC100
SFDA Registration: ML0000000093SFDAA00007
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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
ML0000000093SFDAA00007
Authorization ID
GHTF-2019-3483
Status
Active
Expire Date
February 06, 2022
Manufacturer
Model Information
Model ID(s)
10710 10710-C 107100 10712 10714-C18 10715 10716 10718 10720 10724 10726-C48 10730 10730-AMH 10730-C40 10736 10736-KWT 10735-C 10739-C 10739-C1 10740 10745 10755 10748 10750 10751-C 10754 10754-C 10772 10755-SGH 10756 10763-C 10760-C 10760-AMH 10707 10776
Product Accessories

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