"Fujifilm" electronic bronchoscope
Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION·Registered Mar 10, 2023 – Mar 10, 2028Active- Analysis ID
- c85c9784cbf6dbc9ebb78d3cfcd45d73
- Customs Code
- DHA05603643500
- Manufacturer Country
- Japan
- Authorized Representative
- FUJIFILM HEALTHCARE TAIWAN CO., LTD.
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4680 Bronchial tubescopes (soft or rigid) and accessories thereof
- Import Information
- import
- Registration Date
- Mar 10, 2023
- Expiry Date
- Mar 10, 2028
Top companies providing products similar to ""Fujifilm" electronic bronchoscope"
Recently registered similar products
Access comprehensive regulatory information for "Fujifilm" electronic bronchoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c85c9784cbf6dbc9ebb78d3cfcd45d73 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION, and 2 recent registrations in the same category. 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.