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Philips Xcelera - SFDA Registration ME0000003237SFDAA00052

Access comprehensive regulatory information for Philips Xcelera 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 ME0000003237SFDAA00052 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.

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Class IIa
ME0000003237SFDAA00052
Philips Xcelera
SFDA Registration: ME0000003237SFDAA00052
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Product Information

Workstation ,Picture archiving and communication system ,software

Product Use

Philips Xcelera software product is an integrated multimodality image and information system designed to perform import, export, storage, archiving, review, analysis, quantification, reporting and database management of digital medical images.

Device Classification
Risk Class
Class IIa
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000003237SFDAA00052
Authorization ID
GHTF-2017-1141
Status
Active
Expire Date
September 01, 2020
Manufacturer
Model Information
Model ID(s)
Xcelera
Product Accessories

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