Taiwan FDA registration 176f65b23302f8c847ea2f38eb758390
“Ace” Manual surgical instrument for general use (Non-sterile)
TW: “艾斯”一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·ACE KOREA MEDICAL CO., LTD.·Registered May 12, 2014 – May 12, 2019CancelledRegistration details
- Analysis ID
- 176f65b23302f8c847ea2f38eb758390
- License Form
- Ministry of Health Medical Device Import No. 014124
- Customs Code
- DHA09401412404
Company information
- Manufacturer
- ACE KOREA MEDICAL CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- LA MED INTERNATIONAL 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
- May 12, 2014
- Expiry Date
- May 12, 2019
- Cancellation Date
- Aug 20, 2015
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for “Ace” 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 176f65b23302f8c847ea2f38eb758390 and manufactured by ACE KOREA MEDICAL CO., LTD.. The authorized representative in Taiwan is LA MED INTERNATIONAL CO., LTD..
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