Taiwan FDA registration 7a31205e92163f618680cbe8289a941f
"Yatrien" Cleavey perfused the PTFE balloon catheter
TW: “亞翠恩”克里衛灌注聚四氟乙烯氣球導管
Taiwan·Risk Class 2·ATRIUM MEDICAL CORPORATION·Registered Sep 25, 2008 – Sep 25, 2013CancelledRegistration details
- Analysis ID
- 7a31205e92163f618680cbe8289a941f
- Customs Code
- DHA00601923104
Company information
- Manufacturer
- ATRIUM MEDICAL CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- Hong Kong Synmei Co., Ltd. Taiwan Branch
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.5150 血栓切除術導管
- Import Information
- import
Dates and status
- Registration Date
- Sep 25, 2008
- Expiry Date
- Sep 25, 2013
- Cancellation Date
- Aug 13, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Yatrien" Cleavey perfused the PTFE balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7a31205e92163f618680cbe8289a941f and manufactured by ATRIUM MEDICAL CORPORATION. The authorized representative in Taiwan is Hong Kong Synmei Co., Ltd. Taiwan Branch.
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