Taiwan FDA registration de7c64dad5855eca94a8f7eb7b1ac416
"Graceful" mitral and aortic valve balloon dilation catheters
TW: “優美”二尖瓣及主動脈瓣氣球擴張導管
Taiwan·Risk Class 2·NUMED CANADA INC.;; NUMED INC.·Registered Mar 09, 2007 – Mar 09, 2027ActiveRegistration details
- Analysis ID
- de7c64dad5855eca94a8f7eb7b1ac416
- Customs Code
- DHA00601778205
Company information
- Manufacturer
- NUMED CANADA INC.;; NUMED INC.
- Manufacturer Country
- Canada;;United States
- Authorized Representative
- SILVER BELL ENTERPRISE INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Mar 09, 2007
- Expiry Date
- Mar 09, 2027
About this record
Access comprehensive regulatory information for "Graceful" mitral and aortic valve balloon dilation catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number de7c64dad5855eca94a8f7eb7b1ac416 and manufactured by NUMED CANADA INC.;; NUMED INC.. The authorized representative in Taiwan is SILVER BELL ENTERPRISE 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