Taiwan FDA registration 5e55fcdb1305f304b52069a7006477a5
"Cottman" bone forceps
TW: "柯特曼" 骨鉗
Taiwan·Risk Class 2·CODMAN & SHURTLEFF,INC.·Registered Oct 12, 2005 – Oct 12, 2015CancelledRegistration details
- Analysis ID
- 5e55fcdb1305f304b52069a7006477a5
- Customs Code
- DHA00601266604
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
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.4840 Manual bone flower
- Import Information
- import
Dates and status
- Registration Date
- Oct 12, 2005
- Expiry Date
- Oct 12, 2015
- Cancellation Date
- Aug 09, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Cottman" bone forceps in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5e55fcdb1305f304b52069a7006477a5 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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