Omnisilk - SFDA Registration ME0000001558SFDAA00240
Access comprehensive regulatory information for Omnisilk 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 ME0000001558SFDAA00240 and manufactured by PAUL HARTMANN AG.
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
ME0000001558SFDAA00240
Omnisilk
SFDA Registration: ME0000001558SFDAA00240
Product Information
Adhesive tape
Product Use
Fixation and covering of wound dressings
Device Classification
Risk Class
Class I
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000001558SFDAA00240
Authorization ID
GHTF-2014-0091
Status
Active
Expire Date
April 02, 2017
Manufacturer
Manufacturer Name
PAUL HARTMANN AGModel Information
Model ID(s)
900418
900419
900420
900430
900431
900432
Product Accessories
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