Taiwan FDA registration 1630076e79ac51562a3631e3ad07ff76
“Hexacath” Peripheral Vascular Stent HELIOS SD Ti
TW: “海斯凱”哈里歐-鈦周邊血管支架
Taiwan·Risk Class 2·MD·HEXACATH·Registered Jun 17, 2015 – Jun 17, 2025ExpiredRegistration details
- Analysis ID
- 1630076e79ac51562a3631e3ad07ff76
- License Form
- Ministry of Health Medical Device Import No. 027428
- Customs Code
- DHA05602742802
Company information
- Manufacturer
- HEXACATH
- Manufacturer Country
- France
- Authorized Representative
- CATHERINE CONSULTANTS CO., LTD.
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)
- E0001 Cardiovascular stents
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 17, 2015
- Expiry Date
- Jun 17, 2025
About this record
Access comprehensive regulatory information for “Hexacath” Peripheral Vascular Stent HELIOS SD Ti in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1630076e79ac51562a3631e3ad07ff76 and manufactured by HEXACATH. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..
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