"Fujino" electronic endoscope
Taiwan·Risk Class 2·FUJINON MITO CORPORATION;; FUJIFILM CORPORATION·Registered Jul 21, 2006 – Jul 21, 2021Cancelled- Analysis ID
- 66e245785061b4208806f0d6e60bc61f
- Customs Code
- DHA00601689602
- Manufacturer
- FUJINON MITO CORPORATION;; FUJIFILM CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- WELMORE 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
- Jul 21, 2006
- Expiry Date
- Jul 21, 2021
- Cancellation Date
- Aug 15, 2023
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Fujino" electronic endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 66e245785061b4208806f0d6e60bc61f and manufactured by FUJINON MITO CORPORATION;; FUJIFILM CORPORATION. The authorized representative in Taiwan is WELMORE CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUJIFILM Healthcare Manufacturing Corporation Hitachiomiya 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.