Taiwan FDA registration 8f730074ec100f48e6231a3e9b0ebb37
Ganak Pushima pelvic floor repair system
TW: 蓋那客普席瑪骨盆底修復系統
Taiwan·Risk Class 2·ETHICON SARL·Registered Jun 30, 2010 – Jun 30, 2015CancelledRegistration details
- Analysis ID
- 8f730074ec100f48e6231a3e9b0ebb37
- Customs Code
- DHA00602118005
Company information
- Manufacturer
- ETHICON SARL
- Manufacturer Country
- Switzerland
- 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)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.3300 Surgical mesh
- Import Information
- import
Dates and status
- Registration Date
- Jun 30, 2010
- Expiry Date
- Jun 30, 2015
- Cancellation Date
- Jan 15, 2015
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Ganak Pushima pelvic floor repair system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8f730074ec100f48e6231a3e9b0ebb37 and manufactured by ETHICON SARL. The authorized representative in Taiwan is Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch.
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