Taiwan FDA registration 179ec77a25276e5592ff8a8d0c73e21e
"Fujino" bronchoscope
TW: "富士能" 支氣管鏡
Taiwan·Risk Class 2·FUJINON MITO CORPORATION·Registered Nov 17, 2005 – Nov 17, 2020CancelledRegistration details
- Analysis ID
- 179ec77a25276e5592ff8a8d0c73e21e
- Customs Code
- DHA00601357802
Company information
- Manufacturer
- FUJINON MITO CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- WELMORE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4680 Bronchial tubescopes (soft or rigid) and accessories thereof
- Import Information
- import
Dates and status
- Registration Date
- Nov 17, 2005
- Expiry Date
- Nov 17, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Fujino" bronchoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 179ec77a25276e5592ff8a8d0c73e21e and manufactured by FUJINON MITO CORPORATION. The authorized representative in Taiwan is WELMORE CO., LTD..
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