Taiwan FDA registration 9e5a2f622f0dd5344dde04ac8260bcc9
"Renewal" Dental Hand Instruments (Unsterilized)
TW: "維新" 牙科手用器械 (未滅菌)
Taiwan·Risk Class 1·HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.·Registered Sep 11, 2013 – Sep 11, 2018CancelledRegistration details
- Analysis ID
- 9e5a2f622f0dd5344dde04ac8260bcc9
Company information
- Manufacturer
- HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Restoration Management Consultants Limited
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 Dentistry
- Product Type (Level 2)
- F.4565 牙科手用器械
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Sep 11, 2013
- Expiry Date
- Sep 11, 2018
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Renewal" Dental Hand Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9e5a2f622f0dd5344dde04ac8260bcc9 and manufactured by HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is Restoration Management Consultants Limited.
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