Taiwan FDA registration aa80ec71f0cf697a188487aee834c161

“DENTAMERICA” Premier Diamond Instrument (Non-Sterile)

TW: “登特美”牙科用鑽石器械 (未滅菌)

Taiwan·Risk Class 1·MD·Qiqi Technology Co., Ltd. Xizhi factory·Registered Aug 21, 2019 – Aug 21, 2024Expired

Registration details

Analysis ID: aa80ec71f0cf697a188487aee834c161
License Form: Ministry of Health Medical Device Manufacturing No. 007909

Company information

Manufacturer: Qiqi Technology Co., Ltd. Xizhi factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Qiqi Technology Co., Ltd. Xizhi factory

Product details

Intended Use: Limited to the first level identification range of dental diamond instruments (F.4535) under the Measures for the Administration of Medical Equipment.
Product Type (Level 1): F Dental devices
Product Type (Level 2): F4535 Dental Diamond Instruments
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Aug 21, 2019
Expiry Date: Aug 21, 2024

About this record

Access comprehensive regulatory information for “DENTAMERICA” Premier Diamond 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 aa80ec71f0cf697a188487aee834c161 and manufactured by Qiqi Technology Co., Ltd. Xizhi factory. The authorized representative in Taiwan is Qiqi Technology Co., Ltd. Xizhi factory.

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