Saudi Arabia SFDA registration ME0000003237SFDAA00053
ViewForum R6.3V1
Product information
Image Processing Software
Product use
ViewForum software receives image data from medical scanning devices, such as CT and MRI, or from image archives. ViewForum performs viewing, image manipulation, communication, printing, and quantification of images.
Device classification
- Risk Class
- Class IIa
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000003237SFDAA00053
- Authorization ID
- GHTF-2017-1142
- Status
- Active
- Expire Date
- February 01, 2023
Manufacturer
- Manufacturer Name
- Philips Medical Systems Nederland B.V.
Model information
- Model ID(s)
- Version 6.3.X.XX
Product accessories
[]
About this record
Access comprehensive regulatory information for ViewForum R6.3V1 in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIa device is registered with Saudi Arabia SFDA under registration number ME0000003237SFDAA00053 and manufactured by Philips Medical Systems Nederland B.V..
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 IIa