"Covidien" endoscopic automatic vascular clamp
Taiwan·Risk Class 2·COVIDIEN LLC;; COVID·Registered Jan 21, 2013 – Jan 21, 2018Cancelled- Analysis ID
- b2817ebcb52ffc8b03ebf6f9b8e332a7
- Customs Code
- DHA00602445902
- Manufacturer
- COVIDIEN LLC;; COVID
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4300 Implantable Clips
- Import Information
- import
- Registration Date
- Jan 21, 2013
- Expiry Date
- Jan 21, 2018
- Cancellation Date
- Dec 13, 2019
- Status
- Logged out
- Reason
- 許可證已逾有效期
Top companies providing products similar to ""Covidien" endoscopic automatic vascular clamp"
Recently registered similar products
Access comprehensive regulatory information for "Covidien" endoscopic automatic vascular clamp in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b2817ebcb52ffc8b03ebf6f9b8e332a7 and manufactured by COVIDIEN LLC;; COVID. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including COVIDIEN LLC;; Covidien, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.