Taiwan FDA registration 07cbf68402a79532e67b2c3cbe8c23a8
"Caudix" Tertisso transradial epithelial sheath guide
TW: “考迪斯”雷帝索經橈骨皮膜鞘導引器
Registration details
- Analysis ID
- 07cbf68402a79532e67b2c3cbe8c23a8
- Customs Code
- DHA00602447908
Company information
- Manufacturer
- GREATBATCH MEDICAL INC
- Manufacturer Country
- United States
- Authorized Representative
- Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) 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.1340 Catheter Introducers
- Import Information
- import
Dates and status
- Registration Date
- Feb 22, 2013
- Expiry Date
- Feb 22, 2018
- Cancellation Date
- Nov 15, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Caudix" Tertisso transradial epithelial sheath guide in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 07cbf68402a79532e67b2c3cbe8c23a8 and manufactured by GREATBATCH MEDICAL INC. The authorized representative in Taiwan is Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch.
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