Taiwan FDA registration 29ba20153a9c97c5130ba1d3f878fc44
Rotary aorta punch (sterilization)
TW: “奧圖”旋轉式主動脈打孔器 (滅菌)
Taiwan·Risk Class 1·ALTO DEVELOPMENT CORPORATION·Registered Apr 06, 2010 – Apr 06, 2030ActiveRegistration details
- Analysis ID
- 29ba20153a9c97c5130ba1d3f878fc44
- Customs Code
- DHA04400868105
Company information
- Manufacturer
- ALTO DEVELOPMENT CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- ZIMMER BIOMET TAIWAN CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, the first level identification range of cardiovascular surgical instruments (E.4500).
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.4500 心臟血管外科器械
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Apr 06, 2010
- Expiry Date
- Apr 06, 2030
About this record
Access comprehensive regulatory information for Rotary aorta punch (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 29ba20153a9c97c5130ba1d3f878fc44 and manufactured by ALTO DEVELOPMENT CORPORATION. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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