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"Kaijie" cervical kit - Taiwan Registration c097d88f7f977843dfad8fe4379295fc

Access comprehensive regulatory information for "Kaijie" cervical kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c097d88f7f977843dfad8fe4379295fc and manufactured by QIAGEN. The authorized representative in Taiwan is QIAGEN TAIWAN COMPANY LIMITED.

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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c097d88f7f977843dfad8fe4379295fc
Registration Details
Taiwan FDA Registration: c097d88f7f977843dfad8fe4379295fc
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Device Details

"Kaijie" cervical kit
TW: โ€œๅ‡ฑๆฐโ€ๅญๅฎฎ้ ธๆŽกๆชขๅฅ—็ต„
Risk Class 2

Registration Details

c097d88f7f977843dfad8fe4379295fc

DHA00602423802

Company Information

United States

Product Details

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

l Obstetrics and Gynecology

L.4530 ๅฉฆ็”ข็ง‘ๅฐˆ็”จๆ‰‹ๅ‹•ๅ™จๆขฐ

import

Dates and Status

Nov 29, 2012

Nov 29, 2027