Taiwan FDA registration 2871894fbdb6ce3daa494149dfd1b30b
“CareFusion” Manual Surgical Instrument for General Use (Non-Sterile)
TW: "凱飛峻" 一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·CAREFUSION 209, INC.·Registered Mar 05, 2014 – Mar 05, 2019CancelledRegistration details
- Analysis ID
- 2871894fbdb6ce3daa494149dfd1b30b
- License Form
- Ministry of Health Medical Device Import No. 013913
- Customs Code
- DHA09401391300
Company information
- Manufacturer
- CAREFUSION 209, INC.
- Manufacturer Country
- Slovakia
- Authorized Representative
- SYNGROWTH CO., LTD.
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
- Mar 05, 2014
- Expiry Date
- Mar 05, 2019
- 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 “CareFusion” 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 2871894fbdb6ce3daa494149dfd1b30b and manufactured by CAREFUSION 209, INC.. The authorized representative in Taiwan is SYNGROWTH CO., LTD..
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