Taiwan FDA registration a430b69da6df0228aa6d9434979f6c63
“InspireMD” CGuard Carotid Embolic Prevention Stent System
TW: “醫沛美”栓塞防護支架系統
Taiwan·Risk Class 3·MD·InspireMD Ltd·Registered Nov 10, 2021 – Nov 10, 2026ActiveRegistration details
- Analysis ID
- a430b69da6df0228aa6d9434979f6c63
- License Form
- Ministry of Health Medical Device Import No. 034603
- Customs Code
- DHA05603460308
Company information
- Manufacturer
- InspireMD Ltd
- Manufacturer Country
- Israel
- Authorized Representative
- LORION ENTERPRISES INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E0001 Cardiovascular stents
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 10, 2021
- Expiry Date
- Nov 10, 2026
About this record
Access comprehensive regulatory information for “InspireMD” CGuard Carotid Embolic Prevention Stent System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a430b69da6df0228aa6d9434979f6c63 and manufactured by InspireMD Ltd. The authorized representative in Taiwan is LORION ENTERPRISES INC..
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