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"Mitoyo" shadowless surgical light - Taiwan Registration 36f5d4af74bbf665161f3f3fbd712d77

Access comprehensive regulatory information for "Mitoyo" shadowless surgical light in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 36f5d4af74bbf665161f3f3fbd712d77 and manufactured by BENQ MEDICAL TECHNOLOGY CORPORATION. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.

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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36f5d4af74bbf665161f3f3fbd712d77
Registration Details
Taiwan FDA Registration: 36f5d4af74bbf665161f3f3fbd712d77
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Device Details

"Mitoyo" shadowless surgical light
TW: โ€œไธ‰่ฑโ€็„กๅฝฑๅค–็ง‘ๆ‰‹่ก“็‡ˆ
Risk Class 2
Cancelled

Registration Details

36f5d4af74bbf665161f3f3fbd712d77

DHY00500335001

Company Information

Taiwan, Province of China

Product Details

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

I General, Plastic Surgery and Dermatology

I.4580 Surgical lamp

Domestic

Dates and Status

Jul 19, 2011

Jul 19, 2016

May 28, 2018

Cancellation Information

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