"Medtronic" Sherpa guide tube
Taiwan·Risk Class 2·MEDTRONIC VASCULAR·Registered Jul 04, 2008 – Jul 04, 2023Cancelled- Analysis ID
- fe8e09ce7ce7773f9ac5e4d284f3fcec
- Customs Code
- DHA00601909203
- 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
- Jul 04, 2008
- Expiry Date
- Jul 04, 2023
- Cancellation Date
- Jan 08, 2020
- Status
- Logged out
- Reason
- 自請註銷
Top companies providing products similar to ""Medtronic" Sherpa guide tube"
Recently registered similar products
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 fe8e09ce7ce7773f9ac5e4d284f3fcec 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.