Taiwan FDA registration 41cfc97f3f707fccd5c9f2a63f3fadb6
“Abbott” Hi-Torque Cross-IT XT Guide Wire
TW: “亞培”高鐸格擴司通導管引線
Taiwan·Risk Class 2·MD·ABBOTT VASCULAR·Registered Dec 26, 2016 – Dec 26, 2026ActiveRegistration details
- Analysis ID
- 41cfc97f3f707fccd5c9f2a63f3fadb6
- License Form
- Ministry of Health Medical Device Import No. 029258
- Customs Code
- DHA05602925800
Company information
- Manufacturer
- ABBOTT VASCULAR
- Manufacturer Country
- United States
- Authorized Representative
- Abbott Medical Taiwan Co.
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
- Dec 26, 2016
- Expiry Date
- Dec 26, 2026
About this record
Access comprehensive regulatory information for “Abbott” Hi-Torque Cross-IT XT 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 41cfc97f3f707fccd5c9f2a63f3fadb6 and manufactured by ABBOTT VASCULAR. The authorized representative in Taiwan is Abbott Medical Taiwan Co..
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