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“Gyrus”Nasopharyngeal catheter(Non-sterile) - Taiwan Registration 196aa9eb21dd99c39a9df9ecd9dc945c

Access comprehensive regulatory information for “Gyrus”Nasopharyngeal catheter(Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 196aa9eb21dd99c39a9df9ecd9dc945c and manufactured by GYRUS MEDICAL GMBH. The authorized representative in Taiwan is Yuanyou Industrial 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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196aa9eb21dd99c39a9df9ecd9dc945c
Registration Details
Taiwan FDA Registration: 196aa9eb21dd99c39a9df9ecd9dc945c
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Device Details

“Gyrus”Nasopharyngeal catheter(Non-sterile)
TW: “吉洛氏”鼻咽部導管 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

196aa9eb21dd99c39a9df9ecd9dc945c

Ministry of Health Medical Device Import No. 013487

DHA09401348709

Company Information

Germany

Product Details

G ENT device

G4175 Nasopharyngeal conduit

Imported from abroad

Dates and Status

Oct 09, 2013

Oct 09, 2018

Aug 05, 2022

Cancellation Information

Logged out

未展延而逾期者