Taiwan FDA registration cdb5c0437d3b9af9a387a6a3c3dc3b90
"Covidien" trocar needle
TW: "柯惠" 套管針
Taiwan·Risk Class 2·COVIDIEN LLC;; COVIDIEN IRELAND LIMITED·Registered Nov 15, 2005 – Nov 15, 2015CancelledRegistration details
- Analysis ID
- cdb5c0437d3b9af9a387a6a3c3dc3b90
- Customs Code
- DHA00601298000
Company information
- Manufacturer
- COVIDIEN LLC;; COVIDIEN IRELAND LIMITED
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- Taiwan Covidien Corporation Limited
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Nov 15, 2005
- Expiry Date
- Nov 15, 2015
- Cancellation Date
- Mar 16, 2017
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Covidien" trocar needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cdb5c0437d3b9af9a387a6a3c3dc3b90 and manufactured by COVIDIEN LLC;; COVIDIEN IRELAND LIMITED. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.
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