Singapore HSA registration DE0510102
Fujifilm Fujifilm Processor EP-8000
Singapore·CLASS B·Fujifilm Corporation·Registered December 03, 2024Device 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 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.
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
About this record
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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