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"Yanbo" spray therapy device - Taiwan Registration 0543d28feb35dd32813ce03bc30cbc1e

Access comprehensive regulatory information for "Yanbo" spray therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0543d28feb35dd32813ce03bc30cbc1e and manufactured by Wellell Inc.. The authorized representative in Taiwan is Wellell Inc..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Wellell Inc., Jibo Co., Ltd.;; APEX MEDICAL (KUNSHAN) CORP., and 5 recent registrations in the same category. 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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0543d28feb35dd32813ce03bc30cbc1e
Registration Details
Taiwan FDA Registration: 0543d28feb35dd32813ce03bc30cbc1e
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Device Details

"Yanbo" spray therapy device
TW: โ€œ้›ƒๅšโ€ๅ™ด้œงๆฒป็™‚ๅ™จ
Risk Class 2
Cancelled

Registration Details

0543d28feb35dd32813ce03bc30cbc1e

DHY00500284405

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

D Anesthesiology

D.5630 Nebulizer

Domestic

Dates and Status

Dec 01, 2009

Dec 01, 2014

Jun 08, 2018

Cancellation Information

Logged out

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