Saudi Arabia SFDA registration ME0000001558SFDAA00239
Omnifilm
Saudi Arabia·Medical Device·PAUL HARTMANN AG·Class IActiveProduct 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
- ME0000001558SFDAA00239
- Authorization ID
- GHTF-2017-0274
- Status
- Active
- Expire Date
- April 02, 2020
Manufacturer
- Manufacturer Name
- PAUL HARTMANN AG
Model information
- Model ID(s)
- 900433 900434 900435 900421 900422 900423
Product accessories
[]
About this record
Access comprehensive regulatory information for Omnifilm 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 ME0000001558SFDAA00239 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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