Taiwan FDA registration f7f091bcc97e0ef4d148dbbbcb4878b6

"Corning" lancet (unsterilized)

TW: "康寧" 採血針(未滅菌)

Taiwan·Risk Class 1·ANHUI KANGNING INDUSTRIAL (GROUP) CO., LTD.·Registered Aug 17, 2011 – Aug 17, 2021Cancelled

Registration details

Analysis ID: f7f091bcc97e0ef4d148dbbbcb4878b6
Customs Code: DHA04600143602

Company information

Manufacturer: ANHUI KANGNING INDUSTRIAL (GROUP) CO., LTD.
Manufacturer Country: China
Authorized Representative: LIKWANG INSTRUMENTS CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: Input;; Chinese goods

Dates and status

Registration Date: Aug 17, 2011
Expiry Date: Aug 17, 2021
Cancellation Date: Oct 12, 2023

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Corning" lancet (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f7f091bcc97e0ef4d148dbbbcb4878b6 and manufactured by ANHUI KANGNING INDUSTRIAL (GROUP) CO., LTD.. The authorized representative in Taiwan is LIKWANG INSTRUMENTS CO., LTD..

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