Taiwan FDA registration d1272115be69ccf87c007b752528fd1d
"Termo" Akufoss coronary balloon dilation catheter
TW: “泰爾茂”阿酷佛斯冠狀動脈汽球擴張導管
Taiwan·Risk Class 3·TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION·Registered Mar 13, 2017 – Mar 13, 2027ActiveRegistration details
- Analysis ID
- d1272115be69ccf87c007b752528fd1d
- Customs Code
- DHA05602940905
Company information
- Manufacturer Country
- Japan
- 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
- Product Type (Level 2)
- E.0005.
- Import Information
- import
Dates and status
- Registration Date
- Mar 13, 2017
- Expiry Date
- Mar 13, 2027
About this record
Access comprehensive regulatory information for "Termo" Akufoss coronary balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d1272115be69ccf87c007b752528fd1d and manufactured by TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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