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"Glober" ENT dosing device (unsterilized) - Taiwan Registration 51ef078d96702faed8d86f83f1d15c19

Access comprehensive regulatory information for "Glober" ENT dosing device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 51ef078d96702faed8d86f83f1d15c19 and manufactured by GLOBAL MEDICAL HOLDINGS, LLC. The authorized representative in Taiwan is NSH MEDICAL CORP..

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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51ef078d96702faed8d86f83f1d15c19
Registration Details
Taiwan FDA Registration: 51ef078d96702faed8d86f83f1d15c19
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Device Details

"Glober" ENT dosing device (unsterilized)
TW: "่‘›ๆด›ๆŸ"่€ณ้ผปๅ–‰ไฝˆๆ–ฝ่—ฅ่ฃ็ฝฎ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

51ef078d96702faed8d86f83f1d15c19

DHA04401205001

Company Information

United States

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "ENT Dispensing Devices (G.5220)".

G ENT Science

G.5220 Ear, nose and throat applicators and substances used in conjunction thereof

import

Dates and Status

Aug 09, 2012

Aug 09, 2017

Dec 20, 2019

Cancellation Information

Logged out

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