Taiwan FDA registration d492479ecfc66eb4b0c66bf99ab99664

"Wei Qi" Intraoral Tooth Drill (Unsterilized)

TW: "緯倢" 口內牙鑽頭 (未滅菌)

Taiwan·Risk Class 1·HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.·Registered Apr 30, 2015 – Apr 30, 2020Cancelled

Registration details

Analysis ID: d492479ecfc66eb4b0c66bf99ab99664

Company information

Manufacturer: HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: WEI JIE BIO CO., LTD.

Product details

Intended Use: Limited to the first level recognition range of intraoral tooth drill bits (F.4130) of the Measures for the Administration of Medical Devices.
Product Type (Level 1): F Dentistry
Product Type (Level 2): F.4130 Internal Dental Drill Bits
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: Apr 30, 2015
Expiry Date: Apr 30, 2020
Cancellation Date: Jun 22, 2022

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Wei Qi" Intraoral Tooth Drill (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d492479ecfc66eb4b0c66bf99ab99664 and manufactured by HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is WEI JIE BIO CO., LTD..

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