"Covidien" endoscopic automatic vascular clamp
Taiwan·Risk Class 2·COVIDIEN LLC;; Covidien·Registered Jun 30, 2004 – Jun 30, 2029Active- Analysis ID
- 7133a00d33cf5ea27a11c4a5d2b8680f
- Customs Code
- DHA00601073500
- Manufacturer
- COVIDIEN LLC;; Covidien
- Manufacturer Country
- Dominican Republic;;United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Import Information
- import
- Registration Date
- Jun 30, 2004
- Expiry Date
- Jun 30, 2029
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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 7133a00d33cf5ea27a11c4a5d2b8680f and manufactured by COVIDIEN LLC;; Covidien. 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;; COVID, 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.