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"Morning Yang" battery-operated translucent (unsterilized) - Taiwan Registration 68b8ce9fc9cfb41ac0d40e3673d874b0

Access comprehensive regulatory information for "Morning Yang" battery-operated translucent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 68b8ce9fc9cfb41ac0d40e3673d874b0 and manufactured by Chaoyang Plastic Factory Co., Ltd. The authorized representative in Taiwan is Chaoyang Plastic Factory Co., Ltd.

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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68b8ce9fc9cfb41ac0d40e3673d874b0
Registration Details
Taiwan FDA Registration: 68b8ce9fc9cfb41ac0d40e3673d874b0
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Device Details

"Morning Yang" battery-operated translucent (unsterilized)
TW: โ€œๆœๆšโ€้›ปๆฑ ๅผ้€็…งๅ™จ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

68b8ce9fc9cfb41ac0d40e3673d874b0

Company Information

Taiwan, Province of China

Product Details

It is limited to the first level of identification scope of the "Transilluminator (M.1945)" of the Measures for the Classification and Grading of Medical Devices.

M Ophthalmology

M.1945 Transilluminator

Domestic

Dates and Status

Jan 18, 2008

Jan 18, 2028