Taiwan FDA registration 0fded6e232b0e4262ddba573f6198cd0
"FISSO" Manual surgical instrument for general use (Non-Sterile)
TW: "飛速" 一般手術用手動式器械 (未滅菌)
Registration details
- Analysis ID
- 0fded6e232b0e4262ddba573f6198cd0
- License Form
- Ministry of Health Medical Device Import No. 018901
- Customs Code
- DHA09401890105
Company information
- Manufacturer
- FISSO
- Manufacturer Country
- Switzerland
- Authorized Representative
- CHIN I PAO CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- 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
- Mar 16, 2018
- Expiry Date
- Mar 16, 2023
About this record
Access comprehensive regulatory information for "FISSO" 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 0fded6e232b0e4262ddba573f6198cd0 and manufactured by FISSO. The authorized representative in Taiwan is CHIN I PAO CO., LTD..
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