Saudi Arabia SFDA registration ME0000001558SFDAA00386
Peha-haft
Saudi Arabia·Medical Device·PAUL HARTMANN AG·Class IActiveProduct information
Cohesive conforming bandage, latex free.
Product use
For fixation bandaging and light compression.
Device classification
- Risk Class
- Class I
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000001558SFDAA00386
- Authorization ID
- GHTF-2019-0446
- Status
- Active
- Expire Date
- December 22, 2020
Manufacturer
- Manufacturer Name
- PAUL HARTMANN AG
Model information
- Model ID(s)
- 932449 932444 932450 932445 932452 932446 932441 932447 932442 932448 932443
Product accessories
[]
About this record
Access comprehensive regulatory information for Peha-haft 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 ME0000001558SFDAA00386 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.
Free DatabasePowered by Pure Global AISFDA Official DataClass I