"Covidien" uses absorbable nails alone
Taiwan·Risk Class 2·COVIDIEN LLC;; COVID·Registered Aug 05, 2010 – Aug 05, 2020Cancelled- Analysis ID
- 6bb5367c7580262274793328d809e9b9
- Customs Code
- DHA00602137609
- Manufacturer
- COVIDIEN LLC;; COVID
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
- Intended Use
- This device can be used in less invasive and open surgery (hernia repair) to fix artificial materials to soft tissues.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Import Information
- import
- Registration Date
- Aug 05, 2010
- Expiry Date
- Aug 05, 2020
- Cancellation Date
- Nov 07, 2017
- Status
- Logged out
- Reason
- 自請註銷
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Access comprehensive regulatory information for "Covidien" uses absorbable nails alone in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6bb5367c7580262274793328d809e9b9 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;; 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.