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"Porcelain Rayguang" optical fiber dental light source (unsterilized) - Taiwan Registration 6e937c1410ec917fa8d5893c1e77cc30

Access comprehensive regulatory information for "Porcelain Rayguang" optical fiber dental light source (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6e937c1410ec917fa8d5893c1e77cc30 and manufactured by MEGAFORCE COMPANY LIMITED. The authorized representative in Taiwan is CEREC Asia INC..

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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6e937c1410ec917fa8d5893c1e77cc30
Registration Details
Taiwan FDA Registration: 6e937c1410ec917fa8d5893c1e77cc30
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Device Details

"Porcelain Rayguang" optical fiber dental light source (unsterilized)
TW: "็“ท็‘žๅ…‰" ๅ…‰็บ–็ถญ็‰™็ง‘็”จๅ…‰ๆบ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

6e937c1410ec917fa8d5893c1e77cc30

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;; Contract manufacturing

Dates and Status

May 14, 2018

May 14, 2028