Taiwan FDA registration 6143360fac4a5b631629a8d2a78733b9
"Chanceship" digital flat panel X-ray detector
TW: “康世” 數位平板X光偵測器
Registration details
- Analysis ID
- 6143360fac4a5b631629a8d2a78733b9
- Customs Code
- DHA09200119901
Company information
- Manufacturer Country
- United States;;China
- Authorized Representative
- FAITH BIOMED LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1650 透視X光影像增感管
- Import Information
- Input;; Contract manufacturing;; Chinese goods
Dates and status
- Registration Date
- Feb 05, 2021
- Expiry Date
- Feb 05, 2026
About this record
Access comprehensive regulatory information for "Chanceship" digital flat panel X-ray detector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6143360fac4a5b631629a8d2a78733b9 and manufactured by iRay Technology Taicang Ltd.;; CARESTREAM HEALTH, INC.. The authorized representative in Taiwan is FAITH BIOMED 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