Taiwan FDA registration 6345ac346db1d7fd7ff3426613dd70fa
“Abbott” HI-TORQUE JET Guide Wire
TW: “亞培”高鐸格捷特導線
Taiwan·Risk Class 2·MD·ABBOTT VASCULAR·Registered Mar 13, 2015 – Mar 13, 2025ExpiredRegistration details
- Analysis ID
- 6345ac346db1d7fd7ff3426613dd70fa
- License Form
- Ministry of Health Medical Device Import No. 027222
- Customs Code
- DHA05602722205
Company information
- Manufacturer
- ABBOTT VASCULAR
- Manufacturer Country
- United States
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1330 Catheter Lead
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 13, 2015
- Expiry Date
- Mar 13, 2025
About this record
Access comprehensive regulatory information for “Abbott” HI-TORQUE JET Guide Wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6345ac346db1d7fd7ff3426613dd70fa and manufactured by ABBOTT VASCULAR. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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