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“Medtronic” NuVent Eustachian Tube Dilation Balloon - Taiwan Registration 2500ad9623ffff920b6565bc2325b6ab

Access comprehensive regulatory information for “Medtronic” NuVent Eustachian Tube Dilation Balloon in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2500ad9623ffff920b6565bc2325b6ab and manufactured by MEDTRONIC XOMED, INC.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) 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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Registration Details
Taiwan FDA Registration: 2500ad9623ffff920b6565bc2325b6ab
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Device Details

“Medtronic” NuVent Eustachian Tube Dilation Balloon
TW: “美敦力”紐汎特耳咽管擴張球囊
Risk Class 2
MD

Registration Details

2500ad9623ffff920b6565bc2325b6ab

Ministry of Health Medical Device Import No. 036533

DHA05603653300

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

G ENT Science

G4180 Eustachian tube balloon dilation system

Imported from abroad

Dates and Status

Jun 07, 2023

Jun 07, 2028