Taiwan FDA registration a955fdd43a69ef91ea334d5d4eeb6a87
"Lanxun Medical" coronary artery stent balloon dilation catheter
TW: "藍勳醫療" 冠狀動脈支架氣球擴張導管
Taiwan·BLUE MEDICAL DEVICES B.V.·Registered Mar 04, 2005 – Mar 04, 2010CancelledRegistration details
- Analysis ID
- a955fdd43a69ef91ea334d5d4eeb6a87
- Customs Code
- DHA00601107808
Company information
- Manufacturer
- BLUE MEDICAL DEVICES B.V.
- Manufacturer Country
- Netherlands
- 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 04, 2005
- Expiry Date
- Mar 04, 2010
- Cancellation Date
- Nov 16, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Lanxun Medical" coronary artery stent balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. is registered under number a955fdd43a69ef91ea334d5d4eeb6a87 and manufactured by BLUE MEDICAL DEVICES B.V.. 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