Taiwan FDA registration 88a37c570bfdad0c3e61aa25ab4c4a6a
"Termao" Nobler coronary artery coating stent system
TW: “泰爾茂”諾博樂冠狀動脈塗藥支架系統
Taiwan·Risk Class 3·TERUMO EUROPE N.V.·Registered Jun 28, 2010 – Jun 28, 2020CancelledRegistration details
- Analysis ID
- 88a37c570bfdad0c3e61aa25ab4c4a6a
- Customs Code
- DHA00602122603
Company information
- Manufacturer
- TERUMO EUROPE N.V.
- Manufacturer Country
- Belgium
- Authorized Representative
- TERUMO TAIWAN MEDICAL CO., LTD.
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
- Jun 28, 2010
- Expiry Date
- Jun 28, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Termao" Nobler coronary artery coating 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 88a37c570bfdad0c3e61aa25ab4c4a6a and manufactured by TERUMO EUROPE N.V.. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL 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