Taiwan FDA registration bbbb4fc54ec23fa0c66ba9fedf622d19
“Koelis” TRINITY
TW: “可立”超音波系統及其附件
Taiwan·Risk Class 2·MD·KOELIS·Registered May 08, 2019 – May 08, 2024ExpiredRegistration details
- Analysis ID
- bbbb4fc54ec23fa0c66ba9fedf622d19
- License Form
- Ministry of Health Medical Device Import No. 032603
- Customs Code
- DHA05603260301
Company information
- Manufacturer
- KOELIS
- Manufacturer Country
- France
- Authorized Representative
- TAIWAN MEDICAL SUPPLY, INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1560 ultrasonic echo imaging system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 08, 2019
- Expiry Date
- May 08, 2024
About this record
Access comprehensive regulatory information for “Koelis” TRINITY in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bbbb4fc54ec23fa0c66ba9fedf622d19 and manufactured by KOELIS. The authorized representative in Taiwan is TAIWAN MEDICAL SUPPLY, 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