Taiwan FDA registration f7171db93ccf8ad362fa20e018ae3af7
"Gaynac" urinary incontinence surgery with a sling Ijett system
TW: “蓋那客”尿失禁手術用懸吊帶依捷特系統
Taiwan·Risk Class 2·ETHICON SARL·Registered Feb 24, 2011 – Feb 24, 2026CancelledRegistration details
- Analysis ID
- f7171db93ccf8ad362fa20e018ae3af7
- Customs Code
- DHA00602217902
Company information
- Manufacturer
- ETHICON SARL
- Manufacturer Country
- Switzerland
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
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
- Feb 24, 2011
- Expiry Date
- Feb 24, 2026
- Cancellation Date
- Dec 09, 2021
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Gaynac" urinary incontinence surgery with a sling Ijett system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f7171db93ccf8ad362fa20e018ae3af7 and manufactured by ETHICON SARL. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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