Taiwan FDA registration 60abfc7c2d4e0caf79ace7b02017f0e2

"Renewal" tooth intraosseous implant attachment (unsterilized)

TW: "維新"牙齒骨內植入物附件(未滅菌)

Taiwan·Risk Class 1·HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.·Registered Apr 18, 2018 – Apr 18, 2023Cancelled

Registration details

Analysis ID: 60abfc7c2d4e0caf79ace7b02017f0e2

Company information

Manufacturer: HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: WEI-SHIN BIOTECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first-level identification scope of the Measures for the Administration of Medical Devices "Dental Implant Attachment (F.3980)".
Product Type (Level 1): F Dentistry
Product Type (Level 2): F.3980 Intradental implant manipulation equipment
Import Information: Contract manufacturing;; Domestic

Dates and status

Registration Date: Apr 18, 2018
Expiry Date: Apr 18, 2023
Cancellation Date: Feb 02, 2024

Cancellation information

Status: Logged out
Reason: 屆期未申請展延;;自請註銷

About this record

Access comprehensive regulatory information for "Renewal" tooth intraosseous implant attachment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 60abfc7c2d4e0caf79ace7b02017f0e2 and manufactured by HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is WEI-SHIN BIOTECHNOLOGY CO., LTD..

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