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Fujifilm Fujifilm Processor EP-8000 - HSA Registration DE0510102

Access comprehensive regulatory information for Fujifilm Fujifilm Processor EP-8000 in the Singapore medical device market through Pure Global AI's free database. This CLASS B medical device is registered under HSA registration number DE0510102 and owned by Fujifilm Corporation. The device was registered on December 03, 2024.

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
DE0510102
Fujifilm Fujifilm Processor EP-8000
HSA Registration Number: DE0510102
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Product Description

This product has a light source to supply illumination to the endoscope and a function to supply air and water into the body cavity via the endoscope, providing images captured by the endoscope for diagnosis. Combined with endoscope-related equipment, this product enables centralized operation.

Device Classification
Device Class
CLASS B
Medical Speciality Area
Gastroenterology & Urology
Registration Information
Registration Number
DE0510102
Registration Date
December 03, 2024
Retention Due Date
December 02, 2025
Product Owner
Short Name
Fujifilm Corporation
Address
26-30, Nishiazabu 2-chome, Minato-ku, Tokyo 106-8620, JAPAN
Registrant
Address
10 NEW INDUSTRIAL ROAD, FUJIFILM BUILDING, SINGAPORE 536201
Importer
Address
10 NEW INDUSTRIAL ROAD, FUJIFILM BUILDING, SINGAPORE 536201
Model Information
Model Name(s)
Processor
Model Identifier(s)
EP-8000