Taiwan FDA registration e8d661d544f9e76a9c54429018f5e4d3
“Ultra-Pro II” Needle Guidance Starter Kits
TW: “安創普羅II”超音波針導引器套組
Taiwan·Risk Class 2·MD·CIVCO MEDICAL INSTRUMENTS CO., INC·Registered Jul 30, 2013 – Jul 30, 2028ActiveRegistration details
- Analysis ID
- e8d661d544f9e76a9c54429018f5e4d3
- License Form
- Ministry of Health Medical Device Import No. 025216
- Customs Code
- DHA05602521600
Company information
- Manufacturer
- CIVCO MEDICAL INSTRUMENTS CO., INC
- Manufacturer Country
- United States
- Authorized Representative
- CHINA SPRING TRADING CO., LTD.
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
- Jul 30, 2013
- Expiry Date
- Jul 30, 2028
About this record
Access comprehensive regulatory information for “Ultra-Pro II” Needle Guidance Starter Kits in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e8d661d544f9e76a9c54429018f5e4d3 and manufactured by CIVCO MEDICAL INSTRUMENTS CO., INC. The authorized representative in Taiwan is CHINA SPRING TRADING CO., 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