"Medtronic" Sherpa guide tube
Taiwan·Risk Class 2·MEDTRONIC VASCULAR·Registered Mar 18, 2008 – Mar 18, 2023Cancelled- Analysis ID
- 76e268fbb96f7555d3a4888f43c3aad4
- Customs Code
- DHA00601873402
- Manufacturer
- MEDTRONIC VASCULAR
- 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)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
- Registration Date
- Mar 18, 2008
- Expiry Date
- Mar 18, 2023
- Cancellation Date
- Jan 02, 2020
- Status
- Logged out
- Reason
- 自請註銷
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Access comprehensive regulatory information for "Medtronic" Sherpa guide tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 76e268fbb96f7555d3a4888f43c3aad4 and manufactured by MEDTRONIC VASCULAR. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MEDTRONIC VASCULAR, 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.