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"Renqi" pneumoperitoneum needle - Taiwan Registration b80c859e7b3a153ea3e598447006331d

Access comprehensive regulatory information for "Renqi" pneumoperitoneum needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b80c859e7b3a153ea3e598447006331d 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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b80c859e7b3a153ea3e598447006331d
Registration Details
Taiwan FDA Registration: b80c859e7b3a153ea3e598447006331d
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Device Details

"Renqi" pneumoperitoneum needle
TW: โ€œไป้ฝŠโ€ๆฐฃ่…น้‡
Risk Class 2
Cancelled

Registration Details

b80c859e7b3a153ea3e598447006331d

DHY00500293801

Company Information

Taiwan, Province of China

Product Details

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

l Obstetrics and Gynecology

L.1720 Gynecology and gynecologic laparoscopes and their appendages

Domestic

Dates and Status

May 07, 2010

May 07, 2015

May 28, 2018

Cancellation Information

Logged out

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