Taiwan FDA registration 438152b4b1ea91f5f1f3b9b984a4e87c
"Termao" Luma coronary balloon dilation catheter
TW: “泰爾茂”流麗冠狀動脈氣球擴張導管
Taiwan·Risk Class 3·TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION·Registered Dec 11, 2018 – Dec 11, 2028ActiveRegistration details
- Analysis ID
- 438152b4b1ea91f5f1f3b9b984a4e87c
- Customs Code
- DHA05603186602
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
- Dec 11, 2018
- Expiry Date
- Dec 11, 2028
About this record
Access comprehensive regulatory information for "Termao" Luma 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 438152b4b1ea91f5f1f3b9b984a4e87c 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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