Taiwan FDA registration 9e807098e7b40b12227a0c5845e8ba83
"Fujita" Manual Surgical Instrument for General Use (Non-Sterile)
TW: "富士達" 一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·FUJITA MEDICAL INSTRUMENTS CO., LTD.·Registered Jul 22, 2014 – Jul 22, 2019CancelledRegistration details
- Analysis ID
- 9e807098e7b40b12227a0c5845e8ba83
- License Form
- Ministry of Health Medical Device Import No. 014351
- Customs Code
- DHA09401435102
Company information
- Manufacturer
- FUJITA MEDICAL INSTRUMENTS CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- MATECH HEALTHCARE CORPORATION
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 22, 2014
- Expiry Date
- Jul 22, 2019
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Fujita" Manual Surgical Instrument for General Use (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9e807098e7b40b12227a0c5845e8ba83 and manufactured by FUJITA MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is MATECH HEALTHCARE CORPORATION.
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