Taiwan FDA registration e3d71e21c5762573a3512aa372ff8f1d

"BenQ" Dental hand instrument (Non-Sterile)

TW: "明基三豐" 牙科手用器械(未滅菌)

Taiwan·Risk Class 1·MD·BenQ Sanfeng Medical Equipment Co., Ltd. Taichung Factory·Registered May 11, 2018 – May 11, 2023Expired

Registration details

Analysis ID: e3d71e21c5762573a3512aa372ff8f1d
License Form: Ministry of Health Medical Device Manufacturing No. 007247

Company information

Manufacturer: BenQ Sanfeng Medical Equipment Co., Ltd. Taichung Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: BENQ MEDICAL TECHNOLOGY CORPORATION

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".
Product Type (Level 1): F Dental devices
Product Type (Level 2): F4565 Hand instruments for dental use
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: May 11, 2018
Expiry Date: May 11, 2023

About this record

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.

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