Taiwan FDA registration 5bc73283bca4a131c20ac9e90f07c98a
"Yatrien" Cleaved exchange therapy with perfusion catheter
TW: “亞翠恩”克里衛交換治療用灌注導管
Taiwan·Risk Class 2·ATRIUM MEDICAL CORPORATION·Registered Sep 25, 2008 – Sep 25, 2013CancelledRegistration details
- Analysis ID
- 5bc73283bca4a131c20ac9e90f07c98a
- Customs Code
- DHA00601923400
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.1250 Percutaneous catheters
- 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" Cleaved exchange therapy with perfusion catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5bc73283bca4a131c20ac9e90f07c98a and manufactured by ATRIUM MEDICAL CORPORATION. The authorized representative in Taiwan is Hong Kong Synmei Co., Ltd. Taiwan Branch.
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