Taiwan FDA registration 6577be9a0f29849059632ea00ca6a938
HI-TORQUE Proceed Guide Wire
TW: 高鐸格波西血管導線
Registration details
- Analysis ID
- 6577be9a0f29849059632ea00ca6a938
- License Form
- Ministry of Health Medical Device Import No. 034549
- Customs Code
- DHA05603454902
Company information
- Manufacturer
- ABBOTT VASCULAR
- Manufacturer Country
- United States
- Authorized Representative
- Abbott Medical Taiwan Co.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1330 Catheter Lead
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 09, 2021
- Expiry Date
- Jun 09, 2026
About this record
Access comprehensive regulatory information for HI-TORQUE Proceed 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 6577be9a0f29849059632ea00ca6a938 and manufactured by ABBOTT VASCULAR. The authorized representative in Taiwan is Abbott Medical Taiwan Co..
This page provides complete technical specifications, regulatory compliance details. 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.
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