"Medtronic" suction catheter
- Analysis ID
- d8df103d09c0392f7e3f4f2148149bcf
- Customs Code
- DHA00601821909
- 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.5150 血栓切除術導管
- Import Information
- import
- Registration Date
- Aug 24, 2007
- Expiry Date
- Aug 24, 2017
- Cancellation Date
- Dec 13, 2019
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Medtronic" suction catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d8df103d09c0392f7e3f4f2148149bcf 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.