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FUJIFILM FDR SE CONSOLE ( DR-ID 330CL ) Application software - HSA Registration DE0505757

Access comprehensive regulatory information for FUJIFILM FDR SE CONSOLE ( DR-ID 330CL ) Application software in the Singapore medical device market through Pure Global AI's free database. This CLASS B medical device is registered under HSA registration number DE0505757 and owned by FUJIFILM CORPORATION. The device was registered on May 05, 2021.

This page provides complete registration details including product owner information, registrant details, importer information, and regulatory compliance data from the official Singapore HSA medical device database. Pure Global AI offers free access to Singapore's complete medical device registry, helping global MedTech companies navigate HSA regulations efficiently.

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CLASS B
DE0505757
FUJIFILM FDR SE CONSOLE ( DR-ID 330CL ) Application software
HSA Registration Number: DE0505757
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Product Description

Intended to associate digital (for DR) images with patient and exam information, apply image processing to facilitate diagnosis, display the image, and output the resulting image and exam data for further display, distribution, or archiving.

Device Classification
Device Class
CLASS B
Medical Speciality Area
Radiology / Imaging
Registration Information
Registration Number
DE0505757
Registration Date
May 05, 2021
Change Notification Approval Date
November 14, 2024
Retention Due Date
May 04, 2026
Product Owner
Short Name
FUJIFILM
Address
26-30 nishiazabu 2 chome, MINATO-KU TOKYO 106-8620 JAPAN, JAPAN
Registrant
Address
10 NEW INDUSTRIAL ROAD, FUJIFILM BUILDING, SINGAPORE 536201
Importer
Address
10 NEW INDUSTRIAL ROAD, FUJIFILM BUILDING, SINGAPORE 536201 10 NEW INDUSTRIAL ROAD, FUJIFILM BUILDING, SINGAPORE 536201
Model Information
Model Name(s)
DR-ID 330CL Application Software
Model Identifier(s)
DR-ID 330CL