Taiwan FDA registration 943e48b89a0a298690cad16ddc84c502
"Terumo" Artema Stenacomi coronary artery coated stent system
TW: “泰爾茂” 阿提瑪斯特那可米冠狀動脈塗藥支架系統
Taiwan·Risk Class 3·ASHITAKA FACTORY OF TERUMO CORPORATION·Registered Feb 19, 2024 – Feb 19, 2029ActiveRegistration details
- Analysis ID
- 943e48b89a0a298690cad16ddc84c502
- Customs Code
- DHA05603692705
Company information
- Manufacturer
- ASHITAKA FACTORY OF TERUMO CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- TERUMO TAIWAN MEDICAL CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.0001 Cardiovascular stents
- Import Information
- Safety monitoring;; import
Dates and status
- Registration Date
- Feb 19, 2024
- Expiry Date
- Feb 19, 2029
About this record
Access comprehensive regulatory information for "Terumo" Artema Stenacomi coronary artery coated 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 943e48b89a0a298690cad16ddc84c502 and manufactured by ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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