Pure Global

"Baxter" adjustable endoscopic application catheter - Taiwan Registration f6440b9f9b37091061863fd1149747b6

Access comprehensive regulatory information for "Baxter" adjustable endoscopic application catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f6440b9f9b37091061863fd1149747b6 and manufactured by Made (部分製程) in MEXICO;; MICROMEDICS, INC.. The authorized representative in Taiwan is BAXTER HEALTHCARE 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
f6440b9f9b37091061863fd1149747b6
Registration Details
Taiwan FDA Registration: f6440b9f9b37091061863fd1149747b6
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Baxter" adjustable endoscopic application catheter
TW: “百特”可調整式內視鏡應用導管
Risk Class 2

Registration Details

f6440b9f9b37091061863fd1149747b6

DHA05603320007

Company Information

Mexico;;United States

Product Details

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

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

Feb 16, 2020

Feb 16, 2030