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"Bainent" monitoring system before and after production - Taiwan Registration 9a406d5de7e92373671e5792fa2f51c3

Access comprehensive regulatory information for "Bainent" monitoring system before and after production in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9a406d5de7e92373671e5792fa2f51c3 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.

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9a406d5de7e92373671e5792fa2f51c3
Registration Details
Taiwan FDA Registration: 9a406d5de7e92373671e5792fa2f51c3
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Device Details

"Bainent" monitoring system before and after production
TW: "็™พ่ƒฝ็‰น" ็”Ÿ็”ขๅ‰ๅพŒไน‹็›ฃ่ฆ–็ณป็ตฑ
Risk Class 2

Registration Details

9a406d5de7e92373671e5792fa2f51c3

DHA00601268001

Company Information

Korea, Republic of

Product Details

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

l Obstetrics and Gynecology

L.2740 Pre- and post-production monitoring systems and accessories

import

Dates and Status

Oct 13, 2005

Oct 13, 2025