Taiwan FDA registration 44bfe2bae68817bd1aa27b33f4327671
"Abbott" Godor Gconman XVIII vascular leads
TW: “亞培”高鐸格康曼十八血管導線
Registration details
- Analysis ID
- 44bfe2bae68817bd1aa27b33f4327671
- Customs Code
- DHA05603075702
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 Medicine Science
- Product Type (Level 2)
- E.1330 Catheter Guide Wires
- Import Information
- import
Dates and status
- Registration Date
- Mar 08, 2018
- Expiry Date
- Mar 08, 2028
About this record
Access comprehensive regulatory information for "Abbott" Godor Gconman XVIII vascular leads in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 44bfe2bae68817bd1aa27b33f4327671 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.
Free DatabasePowered by Pure Global AI89,000+ Devices