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"BenQ Mitoyo" Medical Inspection Light (Unsterilized) - Taiwan Registration 68a3fb3e04bea20085b2fb458c07f000

Access comprehensive regulatory information for "BenQ Mitoyo" Medical Inspection Light (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 68a3fb3e04bea20085b2fb458c07f000 and manufactured by BenQ Mitoyo Medical Equipment Co., Ltd. Guishan Factory. 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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68a3fb3e04bea20085b2fb458c07f000
Registration Details
Taiwan FDA Registration: 68a3fb3e04bea20085b2fb458c07f000
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Device Details

"BenQ Mitoyo" Medical Inspection Light (Unsterilized)
TW: "ๆ˜ŽๅŸบไธ‰่ฑ" ้†ซ็”จๆชขๆŸฅ็‡ˆ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

68a3fb3e04bea20085b2fb458c07f000

Company Information

Taiwan, Province of China

Product Details

It is limited to the first level of identification scope of the "Optical Fiber Dental Light Source (F.4620)" of the Administrative Measures for the Classification and Classification of Medical Devices.

F Dentistry

F.4620 Light source for optical fiber dentistry

Domestic

Dates and Status

Oct 20, 2015

Oct 20, 2025