"Fujifilm" electronic digestive endoscope
Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION·Registered Oct 22, 2018 – Oct 22, 2028Active- Analysis ID
- 151197decc3c91243686353204467868
- Customs Code
- DHA05603168801
- Manufacturer Country
- Japan
- Authorized Representative
- FUJIFILM HEALTHCARE TAIWAN CO., LTD.
- 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
- Registration Date
- Oct 22, 2018
- Expiry Date
- Oct 22, 2028
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Access comprehensive regulatory information for "Fujifilm" electronic digestive endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 151197decc3c91243686353204467868 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.