Taiwan FDA registration 9524afd1a6431b6cff61f296fd75d8fe
"Cottman" ventricular cannula
TW: "柯特曼" 腦室套管
Registration details
- Analysis ID
- 9524afd1a6431b6cff61f296fd75d8fe
- Customs Code
- DHA04400277204
Company information
- Manufacturer
- CODMAN & SHURTLEFF,INC.
- Manufacturer Country
- United States
- Authorized Representative
- Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch
Product details
- Intended Use
- A ventricular cannula is used to insert the ventricles for aspiration or injection. This device is often referred to as a ventricular needle.
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.4060 Cerebral cannula
- Import Information
- import
Dates and status
- Registration Date
- Mar 02, 2006
- Expiry Date
- Mar 02, 2011
- Cancellation Date
- Nov 27, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Cottman" ventricular cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9524afd1a6431b6cff61f296fd75d8fe and manufactured by CODMAN & SHURTLEFF,INC.. The authorized representative in Taiwan is Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch.
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