Taiwan FDA registration 0f2397bd8ed52aa0d698ab0a722f89c9
Ganak Privum Pelvic Floor Repair System
TW: 蓋那客普利福姆骨盆底修復系統
Registration details
- Analysis ID
- 0f2397bd8ed52aa0d698ab0a722f89c9
- Customs Code
- DHA00602148106
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
- Sep 21, 2010
- Expiry Date
- Sep 21, 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 Privum 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 0f2397bd8ed52aa0d698ab0a722f89c9 and manufactured by ETHICON SARL. 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