Taiwan FDA registration df92c4caff647d207868693396167ec4
"Fuqiang" silicone surgical jaw cap (sterilized)
TW: “富強” 矽膠手術夾鉗口蓋(滅菌)
Registration details
- Analysis ID
- df92c4caff647d207868693396167ec4
Company information
- Manufacturer
- FORTUNE MEDICAL INSTRUMENT CORP.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- FORTUNE MEDICAL INSTRUMENT CORP.
Product details
- Intended Use
- Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- 國產;; QMS/QSD
Dates and status
- Registration Date
- Jan 27, 2022
- Expiry Date
- Jan 27, 2027
About this record
Access comprehensive regulatory information for "Fuqiang" silicone surgical jaw cap (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number df92c4caff647d207868693396167ec4 and manufactured by FORTUNE MEDICAL INSTRUMENT CORP.. The authorized representative in Taiwan is FORTUNE MEDICAL INSTRUMENT CORP..
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