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"Renzi" is poured into the filter tube group (sterilized) - Taiwan Registration 36800dd4df27fdc6ee9e44f179064821

Access comprehensive regulatory information for "Renzi" is poured into the filter tube group (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 36800dd4df27fdc6ee9e44f179064821 and manufactured by TOP-BOUND ENTERPRISE CO., LTD.. The authorized representative in Taiwan is TOP-BOUND 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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36800dd4df27fdc6ee9e44f179064821
Registration Details
Taiwan FDA Registration: 36800dd4df27fdc6ee9e44f179064821
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Device Details

"Renzi" is poured into the filter tube group (sterilized)
TW: โ€œไป้ฝŠโ€็Œๅ…ฅ้Žๆฟพ็ฎก็ต„(ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

36800dd4df27fdc6ee9e44f179064821

Company Information

Taiwan, Province of China

Product Details

Limited to the first level recognition range of laparoscopic perfusion device (L.1730) for the management of medical devices.

l Obstetrics and Gynecology

L.1730 ่…น่…”้ก็Œๅ…ฅๅ™จ

QMS/QSD;; ๅœ‹็”ข

Dates and Status

Jun 30, 2009

Jun 30, 2014

May 28, 2018

Cancellation Information

Logged out

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