Taiwan FDA registration 21847ebf8b7e76d5ae741fadf599dc80
"Kaitai" biphasic positive pressure breathing therapy instrument
TW: “凱迪泰”雙相正壓呼吸治療儀
Taiwan·Risk Class 2·CURATIVE MEDICAL TECHNOLOGY INC (SUZHOU)·Registered Mar 04, 2014 – Mar 04, 2029ActiveRegistration details
- Analysis ID
- 21847ebf8b7e76d5ae741fadf599dc80
- Customs Code
- DHA09200057801
Company information
- Manufacturer
- CURATIVE MEDICAL TECHNOLOGY INC (SUZHOU)
- Manufacturer Country
- China
- Authorized Representative
- RTSYSTEM INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5905 Non-continuous respirators
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Mar 04, 2014
- Expiry Date
- Mar 04, 2029
About this record
Access comprehensive regulatory information for "Kaitai" biphasic positive pressure breathing therapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 21847ebf8b7e76d5ae741fadf599dc80 and manufactured by CURATIVE MEDICAL TECHNOLOGY INC (SUZHOU). The authorized representative in Taiwan is RTSYSTEM INC..
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