Taiwan FDA registration c75ec8068c90a3e19faf0cbdec4faa75
"Cottman" cranial plastic mesh
TW: "柯特曼" 頭顱整形網
Taiwan·Risk Class 2·CODMAN & SHURTLEFF,INC.·Registered Jun 09, 2005 – Jun 09, 2015CancelledRegistration details
- Analysis ID
- c75ec8068c90a3e19faf0cbdec4faa75
- Customs Code
- DHA00601144305
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
- Import Information
- import
Dates and status
- Registration Date
- Jun 09, 2005
- Expiry Date
- Jun 09, 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" cranial plastic mesh in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c75ec8068c90a3e19faf0cbdec4faa75 and manufactured by CODMAN & SHURTLEFF,INC.. The authorized representative in Taiwan is Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices