Pure Global

"Glesine" nasal dilator patch (unsterilized)  - Taiwan Registration e61dc7e58a227e2606e543fe97ab5d48

Access comprehensive regulatory information for "Glesine" nasal dilator patch (unsterilized)  in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e61dc7e58a227e2606e543fe97ab5d48 and manufactured by GLAXOSMITHKLINE CO., LTD.. The authorized representative in Taiwan is Nichimi Pharmaceutical 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
e61dc7e58a227e2606e543fe97ab5d48
Registration Details
Taiwan FDA Registration: e61dc7e58a227e2606e543fe97ab5d48
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Glesine" nasal dilator patch (unsterilized) 
TW: “格來素” 鼻腔擴張貼片 (未滅菌) 
Risk Class 1
Cancelled

Registration Details

e61dc7e58a227e2606e543fe97ab5d48

DHA04400988309

Company Information

Japan

Product Details

Limited to the first level recognition range of the "nasal expander (G.3900)" of the Measures for the Administration of Medical Devices.

G ENT Science

G.3900 Nasal extenders

import

Dates and Status

Jan 31, 2011

Jan 31, 2016

Nov 07, 2017

Cancellation Information

Logged out

許可證已逾有效期