Pure Global

“Ultra-Pro II” Needle Guidance Starter Kits - Taiwan Registration e8d661d544f9e76a9c54429018f5e4d3

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 Database
Powered by Pure Global AI
89,000+ Devices
e8d661d544f9e76a9c54429018f5e4d3
Registration Details
Taiwan FDA Registration: e8d661d544f9e76a9c54429018f5e4d3
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Ultra-Pro II” Needle Guidance Starter Kits
TW: “安創普羅II”超音波針導引器套組
Risk Class 2
MD

Registration Details

e8d661d544f9e76a9c54429018f5e4d3

Ministry of Health Medical Device Import No. 025216

DHA05602521600

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

P Devices for radiology

P1560 ultrasonic echo imaging system

Imported from abroad

Dates and Status

Jul 30, 2013

Jul 30, 2028