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CoreBio MAS Laparoscopic Instrument - Taiwan Registration 6521f56559de6cbe3fbd6e48a120f3db

Access comprehensive regulatory information for CoreBio MAS Laparoscopic Instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6521f56559de6cbe3fbd6e48a120f3db and manufactured by Hexin Biotechnology Co., Ltd. The authorized representative in Taiwan is Hexin Biotechnology 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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6521f56559de6cbe3fbd6e48a120f3db
Registration Details
Taiwan FDA Registration: 6521f56559de6cbe3fbd6e48a120f3db
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Device Details

CoreBio MAS Laparoscopic Instrument
TW: ๅˆๆ–ฐๅ…ง่ฆ–้กๆ‰‹่ก“็”จๅ™จๆขฐ
Risk Class 2
MD
Cancelled

Registration Details

6521f56559de6cbe3fbd6e48a120f3db

Ministry of Health Medical Device Manufacturing No. 006007

Company Information

Taiwan, Province of China

Product Details

H Gastroenterology-urology devices

H1500 endoscope and accessories

Produced in Taiwan, China

Dates and Status

Dec 05, 2017

Dec 05, 2022

May 19, 2023

Cancellation Information

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