Taiwan FDA registration 28f09b0f24d76e50ebcc292a7b996184
CaRDIaRT Electronic stethoscope
TW: 凱迪雅特電子聽診器
Taiwan·Risk Class 2·MD·IMEDIPLUS INC.·Registered Dec 05, 2017 – Dec 05, 2027ActiveRegistration details
- Analysis ID
- 28f09b0f24d76e50ebcc292a7b996184
- License Form
- Ministry of Health Medical Device Manufacturing No. 005958
Company information
- Manufacturer
- IMEDIPLUS INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- IMEDIPLUS INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1875 stethoscope
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Dec 05, 2017
- Expiry Date
- Dec 05, 2027
About this record
Access comprehensive regulatory information for CaRDIaRT Electronic stethoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 28f09b0f24d76e50ebcc292a7b996184 and manufactured by IMEDIPLUS INC.. The authorized representative in Taiwan is IMEDIPLUS 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