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"BenQ" Dental hand instrument (Non-Sterile) - Taiwan Registration e3d71e21c5762573a3512aa372ff8f1d

Access comprehensive regulatory information for "BenQ" Dental hand instrument (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 e3d71e21c5762573a3512aa372ff8f1d and manufactured by BenQ Sanfeng Medical Equipment Co., Ltd. Taichung 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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e3d71e21c5762573a3512aa372ff8f1d
Registration Details
Taiwan FDA Registration: e3d71e21c5762573a3512aa372ff8f1d
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Device Details

"BenQ" Dental hand instrument (Non-Sterile)
TW: "ๆ˜ŽๅŸบไธ‰่ฑ" ็‰™็ง‘ๆ‰‹็”จๅ™จๆขฐ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

e3d71e21c5762573a3512aa372ff8f1d

Ministry of Health Medical Device Manufacturing No. 007247

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".

F Dental devices

F4565 Hand instruments for dental use

Produced in Taiwan, China

Dates and Status

May 11, 2018

May 11, 2023