Taiwan FDA registration b89c9dfeffb64192ba1cff25d4bde48f
"Aidi Test" Cardiovascular Surgery Instruments (Unsterilized)
TW: "愛帝試" 心臟血管外科器械 (未滅菌)
Taiwan·Risk Class 1·INTERNATIONAL TECHNIDYNE CORP.·Registered Apr 08, 2011 – Apr 08, 2016CancelledRegistration details
- Analysis ID
- b89c9dfeffb64192ba1cff25d4bde48f
- Customs Code
- DHA04401016202
Company information
- Manufacturer
- INTERNATIONAL TECHNIDYNE CORP.
- Manufacturer Country
- United States
- Authorized Representative
- GREAT LIFE SCIENCE INC.
Product details
- Intended Use
- Limited to the first level identification range of medical equipment management measures for 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
- import
Dates and status
- Registration Date
- Apr 08, 2011
- Expiry Date
- Apr 08, 2016
- Cancellation Date
- Jun 26, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Aidi Test" Cardiovascular Surgery Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b89c9dfeffb64192ba1cff25d4bde48f and manufactured by INTERNATIONAL TECHNIDYNE CORP.. The authorized representative in Taiwan is GREAT LIFE SCIENCE INC..
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