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ENAYAH-STERILIZATION WRAP - SFDA Registration ML0000000093SFDAA00016

Access comprehensive regulatory information for ENAYAH-STERILIZATION WRAP 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 ML0000000093SFDAA00016 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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Class I
ML0000000093SFDAA00016
ENAYAH-STERILIZATION WRAP
SFDA Registration: ML0000000093SFDAA00016
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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
ML0000000093SFDAA00016
Authorization ID
GHTF-2019-3483
Status
Active
Expire Date
February 06, 2022
Manufacturer
Model Information
Model ID(s)
58039-C 58051-C EN71150 EN71180 EN71200 EN71240 EN71300 EN71360 EN71391-C EN71400 EN71480 EN71480-25 EN71540 EN71480-34 EN71550 EN72550 EN73550 EN71480-50 EN72600 71241 71481 71240 71480 E68012-CW E68024-W E68026-W45 E68036-W E68039-CW E68051-CW EN68036 EN68039 EN68039-50 58040 EN68176 EN68176-50 EN71480-65 58048 EN68048 EN71455-34 EN68054 10754-02 EN72519 EN72519-50
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