Taiwan FDA registration 79dfe821342b6daf0359b1690c58a7b0
Ampraz Twilip catheter
TW: 安普拉茲特維力普導管
Taiwan·Risk Class 2·AGA MEDICAL CORPORATION·Registered Jul 31, 2012 – Jul 31, 2017CancelledRegistration details
- Analysis ID
- 79dfe821342b6daf0359b1690c58a7b0
- Customs Code
- DHA00602391408
Company information
- Manufacturer
- AGA MEDICAL CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Shengyuda Medical Supplies 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.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Jul 31, 2012
- Expiry Date
- Jul 31, 2017
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Ampraz Twilip catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 79dfe821342b6daf0359b1690c58a7b0 and manufactured by AGA MEDICAL CORPORATION. The authorized representative in Taiwan is Taiwan Shengyuda Medical Supplies Co., Ltd.
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