Taiwan FDA registration 66ca055d329d331c2b7fff9c483e6a68
"Qinda" gauze mat (sterilized)
TW: "勤達" 紗布墊 (滅菌)
Registration details
- Analysis ID
- 66ca055d329d331c2b7fff9c483e6a68
- Customs Code
- DHA04600134802
Company information
- Manufacturer
- JIANGXI YA FENG MEDICAL MATERIAL CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- TEAM POWER MEDICAL INSTRUMENT LTD.
Product details
- Intended Use
- Limited to the first level of classification and grading management of medical devices "external use of non-absorbent gauze or sponge balls (I.4014)" identification range.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4014 Non-absorbent cloth or sea balls are used externally
- Import Information
- Input;; QMS/QSD;; Chinese goods
Dates and status
- Registration Date
- Apr 26, 2011
- Expiry Date
- Apr 26, 2026
About this record
Access comprehensive regulatory information for "Qinda" gauze mat (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 66ca055d329d331c2b7fff9c483e6a68 and manufactured by JIANGXI YA FENG MEDICAL MATERIAL CO., LTD.. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT 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