Taiwan FDA registration 5b325f9bd2e3ecb36930376bffe09119
"Fujino" electronic colonoscopy
TW: "富士能"電子式大腸鏡
Registration details
- Analysis ID
- 5b325f9bd2e3ecb36930376bffe09119
- Customs Code
- DHA00601768201
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- FUJIFILM HEALTHCARE TAIWAN CO., LTD.
Product details
- Intended Use
- For details, please refer to the approved version of Chinese copy
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Jan 11, 2007
- Expiry Date
- Jan 11, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Fujino" electronic colonoscopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5b325f9bd2e3ecb36930376bffe09119 and manufactured by FUJIFILM Techno Products Co., Ltd. Mito Site;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices