Pure Global

Suction mucosal excision device of the "Tepu" endoscope - Taiwan Registration d1b826413339a773edd7603eef4b2e8c

Access comprehensive regulatory information for Suction mucosal excision device of the "Tepu" endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d1b826413339a773edd7603eef4b2e8c and manufactured by TOP CORPORATION SHIMOTSUMA FACTORY. The authorized representative in Taiwan is Taiwan TPU 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
d1b826413339a773edd7603eef4b2e8c
Registration Details
Taiwan FDA Registration: d1b826413339a773edd7603eef4b2e8c
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Suction mucosal excision device of the "Tepu" endoscope
TW: "็‰นๆตฆ"ๅ…ง่ฆ–้ก็š„ๅธๅผ•้ป่†œๅˆ‡้™ค็”จๅ…ท
Risk Class 2

Registration Details

d1b826413339a773edd7603eef4b2e8c

DHA00601279604

Company Information

Product Details

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

H Gastroenterology and urology

import

Dates and Status

Oct 31, 2005

Oct 31, 2025