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"Nasal comfort" physiological seawater neti wash (sterilization) - Taiwan Registration 98be246c7abaf67d7182b6619b8fa012

Access comprehensive regulatory information for "Nasal comfort" physiological seawater neti wash (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 98be246c7abaf67d7182b6619b8fa012 and manufactured by URGO LABORATORIES. The authorized representative in Taiwan is ZUELLIG PHARMA, INC..

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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98be246c7abaf67d7182b6619b8fa012
Registration Details
Taiwan FDA Registration: 98be246c7abaf67d7182b6619b8fa012
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Device Details

"Nasal comfort" physiological seawater neti wash (sterilization)
TW: "้ผป่ˆ’้ฉ" ็”Ÿ็†ๆตทๆฐดๆด—้ผปๅ™จ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

98be246c7abaf67d7182b6619b8fa012

DHA09401488704

Company Information

France

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

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Jan 29, 2015

Jan 29, 2020

Jun 22, 2022

Cancellation Information

Logged out

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