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"Nedek" spray unit (unsterilized) - Taiwan Registration 8e38deb913557ce2701a1c0ec3d96879

Access comprehensive regulatory information for "Nedek" spray unit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8e38deb913557ce2701a1c0ec3d96879 and manufactured by NIDEK MEDICAL PRODUCTS, INC.. 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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8e38deb913557ce2701a1c0ec3d96879
Registration Details
Taiwan FDA Registration: 8e38deb913557ce2701a1c0ec3d96879
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Device Details

"Nedek" spray unit (unsterilized)
TW: โ€œ่€ๅพทๅ…‹โ€ๅ™ด้œง่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

8e38deb913557ce2701a1c0ec3d96879

DHA04400475004

Company Information

United States

Product Details

It is limited to the first level of identification of the "Ear, Nose and Throat Pesticide Application Device (G.5220)" of the Medical Device Management Regulations.

G ENT Science

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

import

Dates and Status

Jun 19, 2006

Jun 19, 2016

Jul 03, 2018

Cancellation Information

Logged out

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