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"Kikosei" uterine device (unsterilized) - Taiwan Registration e335db0185fb0f9982e3ab7c74069c87

Access comprehensive regulatory information for "Kikosei" uterine device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e335db0185fb0f9982e3ab7c74069c87 and manufactured by HSI ERH SHENG ENTERPRISE CO., LTD.. The authorized representative in Taiwan is HSI ERH SHENG ENTERPRISE 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.

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e335db0185fb0f9982e3ab7c74069c87
Registration Details
Taiwan FDA Registration: e335db0185fb0f9982e3ab7c74069c87
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Device Details

"Kikosei" uterine device (unsterilized)
TW: โ€œๅ–œๅ…’็”Ÿโ€ๅญๅฎฎๅˆฎๅ™จ ๏ผˆๆœชๆป…่Œ๏ผ‰
Risk Class 1
Cancelled

Registration Details

e335db0185fb0f9982e3ab7c74069c87

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for Obstetrics and Gynecology (L.4530)".

l Obstetrics and Gynecology

L.4530 ๅฉฆ็”ข็ง‘ๅฐˆ็”จๆ‰‹ๅ‹•ๅ™จๆขฐ

Domestic

Dates and Status

Aug 31, 2006

Aug 31, 2016

Jun 25, 2018

Cancellation Information

Logged out

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