Taiwan FDA registration 8ec9fb06b166b831150ccd5a4e31075f
"Covidien" single mouth articular endoscopic stapler
TW: “柯惠”單一切口關節式內視鏡縫合器
Taiwan·Risk Class 2·COVIDIEN LLC;; COVID·Registered Apr 30, 2014 – Apr 30, 2019CancelledRegistration details
- Analysis ID
- 8ec9fb06b166b831150ccd5a4e31075f
- Customs Code
- DHA05602615804
Company information
- Manufacturer
- COVIDIEN LLC;; COVID
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Apr 30, 2014
- Expiry Date
- Apr 30, 2019
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Covidien" single mouth articular endoscopic stapler in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8ec9fb06b166b831150ccd5a4e31075f and manufactured by COVIDIEN LLC;; COVID. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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