Taiwan FDA registration a3b508d22f43a07a11f4590b7c8f169d
"Covidien" endoscopic suture junction thruster
TW: “柯惠”內視鏡縫合結推進器
Taiwan·Risk Class 2·Covidien llc;; Covidien·Registered May 30, 2018 – May 30, 2023CancelledRegistration details
- Analysis ID
- a3b508d22f43a07a11f4590b7c8f169d
- Customs Code
- DHA05603115900
Company information
- Manufacturer
- Covidien llc;; Covidien
- 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
- May 30, 2018
- Expiry Date
- May 30, 2023
- Cancellation Date
- Sep 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Covidien" endoscopic suture junction thruster in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a3b508d22f43a07a11f4590b7c8f169d and manufactured by Covidien llc;; Covidien. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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