Pure Global

IBE V8.0.1 SW Kit - SFDA Registration ME0000003237SFDAA00057

Access comprehensive regulatory information for IBE V8.0.1 SW Kit 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 ME0000003237SFDAA00057 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 Database
Powered by Pure Global AI
SFDA Official Data
Class IIa
ME0000003237SFDAA00057
IBE V8.0.1 SW Kit
SFDA Registration: ME0000003237SFDAA00057
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Information

Image and Information Management Software

Product Use

Processes clinical images from different modalities and enables advanced visualization of the images. When used by qualified personnel, it provides useful diagnostic information.

Device Classification
Risk Class
Class IIa
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000003237SFDAA00057
Authorization ID
GHTF-2017-1143
Status
Active
Expire Date
May 16, 2022
Manufacturer
Model Information
Model ID(s)
IBE V8.0.1 SW Kit
Product Accessories

[]