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"Yanbo" spray therapy device - Taiwan Registration e795d3b01673f41664f8e323220d82bf

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 e795d3b01673f41664f8e323220d82bf 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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e795d3b01673f41664f8e323220d82bf
Registration Details
Taiwan FDA Registration: e795d3b01673f41664f8e323220d82bf
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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

e795d3b01673f41664f8e323220d82bf

DHY00500241508

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

Mar 13, 2008

Aug 10, 2015

Jun 08, 2018

Cancellation Information

Logged out

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