Taiwan FDA registration ab5ac611aa7f952693b9020728a13146

"AXA" lancet (unsterilized)

TW: "安盛" 採血針(未滅菌)

Taiwan·Risk Class 1·Tianjin Huahong Technology Co., Ltd.·Registered Jun 01, 2015 – Jun 01, 2020Cancelled

Registration details

Analysis ID: ab5ac611aa7f952693b9020728a13146
Customs Code: DHA09600241209

Company information

Manufacturer: Tianjin Huahong Technology Co., Ltd.
Manufacturer Country: China
Authorized Representative: IXENSOR 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: Jun 01, 2015
Expiry Date: Jun 01, 2020
Cancellation Date: Jul 15, 2022

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "AXA" 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 ab5ac611aa7f952693b9020728a13146 and manufactured by Tianjin Huahong Technology Co., Ltd.. The authorized representative in Taiwan is IXENSOR CO., LTD..

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