Taiwan FDA registration f054a2b8920a67621d77b04c1a0c16a4
"Implantech" Manual surgical instrument for general use (Non-Sterile)
TW: "恩普泰" 一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·IMPLANTECH ASSOCIATES INC.·Registered Dec 02, 2015 – Dec 02, 2020CancelledRegistration details
- Analysis ID
- f054a2b8920a67621d77b04c1a0c16a4
- License Form
- Ministry of Health Medical Device Import No. 015919
- Customs Code
- DHA09401591909
Company information
- Manufacturer
- IMPLANTECH ASSOCIATES INC.
- Manufacturer Country
- United States
- Authorized Representative
- LYRA 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
- Dec 02, 2015
- Expiry Date
- Dec 02, 2020
- 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 "Implantech" 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 f054a2b8920a67621d77b04c1a0c16a4 and manufactured by IMPLANTECH ASSOCIATES INC.. The authorized representative in Taiwan is LYRA LTD..
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