Taiwan FDA registration 26520ac991bc496a7bc4b4ebc03eee55
"Termo" Atimast coronary artery coating stent system
TW: “泰爾茂”阿提瑪斯特冠狀動脈塗藥支架系統
Taiwan·Risk Class 3·TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION·Registered Jul 17, 2015 – Jul 17, 2025ExpiredRegistration details
- Analysis ID
- 26520ac991bc496a7bc4b4ebc03eee55
- Customs Code
- DHA05602746008
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. The indications were changed to: as detailed as Chinese copy of the imitation order approval (the original copy of the imitation label approved on August 3, 106 is invalidated).
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.0001 Cardiovascular stents
- Import Information
- import
Dates and status
- Registration Date
- Jul 17, 2015
- Expiry Date
- Jul 17, 2025
About this record
Access comprehensive regulatory information for "Termo" Atimast 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 26520ac991bc496a7bc4b4ebc03eee55 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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