Gastrointestinal catheter/endoscope tracking system sensor, body-surface
- Device ID
- 108902
- MHRA Reference Number
- 108902
- Date Registered
- Nov 26, 2024
- Last Updated
- Oct 16, 2024
- Device Type
- General Medical Device
- Devices
- Gastrointestinal catheter/endoscope tracking system sensor, body-surface
- Type
- Class I
- Address
- 26-30 Nishiazabu 2-chome Minato-ku 26-30Tokyo, Japan
- Created Date
- Oct 18, 2021
- Relationship Type
- UK Responsible Person
- Address
- Fujifilm House Whitbread Way Bedford, England, United KingdomPostcode: MK42 0ZE
Devices with a matching generic name or device type registered with MHRA
Additional devices registered by the same manufacturer
Additional devices represented by Fujifilm Healthcare UK Limited in the UK
Gastrointestinal catheter/endoscope tracking system sensor, body-surface is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 108902. The device is manufactured by FUJIFILM Corporation from Japan, classified as General Medical Device. The authorized representative in the UK is Fujifilm Healthcare UK Limited.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.