Taiwan FDA registration a048ca0cec688321b3fddc4b7a22ed09
"Fuji" single-shot use of ball high-frequency knives
TW: “富士”單次用球型高頻刀
Registration details
- Analysis ID
- a048ca0cec688321b3fddc4b7a22ed09
- Customs Code
- DHA00602477805
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- FUJIFILM HEALTHCARE TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- 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
- Mar 12, 2013
- Expiry Date
- Mar 12, 2023
About this record
Access comprehensive regulatory information for "Fuji" single-shot use of ball high-frequency knives in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a048ca0cec688321b3fddc4b7a22ed09 and manufactured by FUJIFILM Techno Products Co., Ltd. Sano 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