Pure Global

"Beinent" fetal echogram monitor - Taiwan Registration 3a9b4fc004b66fb443325d6fec3e30f1

Access comprehensive regulatory information for "Beinent" fetal echogram monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3a9b4fc004b66fb443325d6fec3e30f1 and manufactured by Bionet Co., Ltd.. The authorized representative in Taiwan is MEDWAY BME CORPORATION.

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
3a9b4fc004b66fb443325d6fec3e30f1
Registration Details
Taiwan FDA Registration: 3a9b4fc004b66fb443325d6fec3e30f1
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Beinent" fetal echogram monitor
TW: "็™พ่ƒฝ็‰น" ่ƒŽๅ…’ๅฟƒ้Ÿณๆ่จ˜็›ฃ่ฆ–ๅ™จ
Risk Class 2

Registration Details

3a9b4fc004b66fb443325d6fec3e30f1

DHA00601268100

Company Information

Korea, Republic of

Product Details

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

l Obstetrics and Gynecology

L.2960 INDUSTRIAL ULTRASONIC CONVERTER AND ACCESSORIES

import

Dates and Status

Oct 13, 2005

Oct 13, 2025