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"Jiacheng" poured into the filter tube group (sterilized) - Taiwan Registration 025b1179e08b67f3698f40223c9f8b3f

Access comprehensive regulatory information for "Jiacheng" 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 025b1179e08b67f3698f40223c9f8b3f and manufactured by Jiacheng Seiko Co., Ltd. second factory. The authorized representative in Taiwan is Jiacheng Seiko Co., Ltd. second factory.

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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025b1179e08b67f3698f40223c9f8b3f
Registration Details
Taiwan FDA Registration: 025b1179e08b67f3698f40223c9f8b3f
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Device Details

"Jiacheng" poured into the filter tube group (sterilized)
TW: โ€œไฝณๆ‰ฟโ€ ็Œๅ…ฅ้Žๆฟพ็ฎก็ต„ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

025b1179e08b67f3698f40223c9f8b3f

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

ๅœ‹็”ข;; QMS/QSD

Dates and Status

Oct 11, 2012

Oct 11, 2017

Dec 05, 2019

Cancellation Information

Logged out

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