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"Xinbo" Medical Examination Light (Non-Sterile) - Taiwan Registration 3bcb16dc0c4d214581189891f4bb6e59

Access comprehensive regulatory information for "Xinbo" Medical Examination Light (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3bcb16dc0c4d214581189891f4bb6e59 and manufactured by ALBERT WAESCHLE LTD.. The authorized representative in Taiwan is XIN BO ENTERPRISE 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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3bcb16dc0c4d214581189891f4bb6e59
Registration Details
Taiwan FDA Registration: 3bcb16dc0c4d214581189891f4bb6e59
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Device Details

"Xinbo" Medical Examination Light (Non-Sterile)
TW: "้‘ซๅš" ้†ซ็”จๆชขๆŸฅ็‡ˆ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

3bcb16dc0c4d214581189891f4bb6e59

Ministry of Health Medical Device Import No. 016923

DHA09401692305

Company Information

United Kingdom

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Light Source for Optical Fiber Dentistry (F.4620)".

F Dental devices

F4620 Light source for photofiber dentistry

Imported from abroad

Dates and Status

Aug 24, 2016

Aug 24, 2021