Taiwan FDA registration 87a7208d1323f7240dd8f944d0d4c829

Longteng influenza virus type A and B kit (unsterilized)

TW: 龍騰流行性感冒病毒A型及B型試劑盒(未滅菌)

Taiwan·Risk Class 1·Longteng Biotechnology Co., Ltd·Registered Aug 25, 2009 – Aug 25, 2019Cancelled

Registration details

Analysis ID: 87a7208d1323f7240dd8f944d0d4c829

Company information

Manufacturer: Longteng Biotechnology Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Longteng Biotechnology Co., Ltd

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3330 流感病毒血清試劑
Import Information: Domestic

Dates and status

Registration Date: Aug 25, 2009
Expiry Date: Aug 25, 2019
Cancellation Date: Jun 17, 2023

Cancellation information

Status: Logged out
Reason: 自行鍵入;;許可證已逾有效期

About this record

Access comprehensive regulatory information for Longteng influenza virus type A and B kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 87a7208d1323f7240dd8f944d0d4c829 and manufactured by Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is Longteng Biotechnology Co., Ltd.

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