Taiwan FDA registration 54daf318bf1c511240e8364a84c25839
"Cottman" shunt system implant device
TW: 〝科特曼〞分流系統植入用器械
Taiwan·Risk Class 1·CODMAN & SHURTLEFF,INC.·Registered Sep 16, 2005 – Sep 16, 2010CancelledRegistration details
- Analysis ID
- 54daf318bf1c511240e8364a84c25839
- Customs Code
- DHA04400047300
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
- Surgical equipment used in cerebrospinal fluid shunt transplantation, including instruments that are pierced under the skin so that the shunt components can pass through the hole.
- Product Type (Level 1)
- K Neuroscience
- Import Information
- import
Dates and status
- Registration Date
- Sep 16, 2005
- Expiry Date
- Sep 16, 2010
- 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" shunt system implant device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 54daf318bf1c511240e8364a84c25839 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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