"Fujifilm" electronic duodenoscopy
Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION·Registered Nov 28, 2011 – Nov 28, 2026Active- Analysis ID
- 42c2a61b358410e74d9ad895b721a054
- Customs Code
- DHA00602303101
- 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
- Nov 28, 2011
- Expiry Date
- Nov 28, 2026
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Access comprehensive regulatory information for "Fujifilm" electronic duodenoscopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 42c2a61b358410e74d9ad895b721a054 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..
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