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"Riester" Medical Examination Light (Non-Sterile) - Taiwan Registration 767f8aa03316e76fa9f6c78616b760b7

Access comprehensive regulatory information for "Riester" 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 767f8aa03316e76fa9f6c78616b760b7 and manufactured by RUDOLF RIESTER GMBH. The authorized representative in Taiwan is BOYANG MEDICAL TECHNOLOGY 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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767f8aa03316e76fa9f6c78616b760b7
Registration Details
Taiwan FDA Registration: 767f8aa03316e76fa9f6c78616b760b7
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Device Details

"Riester" Medical Examination Light (Non-Sterile)
TW: "็‘žๅธ" ้†ซ็”จๆชขๆŸฅ็‡ˆ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

767f8aa03316e76fa9f6c78616b760b7

Ministry of Health Medical Device Import No. 017860

DHA09401786002

Company Information

Germany

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

May 19, 2017

May 19, 2027