Taiwan FDA registration 6c7e1ee3f1fa019a0edb4101fc234014

"Torch" adenovirus test set (unsterilized)

TW: "炬合" 腺病毒檢驗試劑組 (未滅菌)

Taiwan·Risk Class 1·HANGZHOU GENESIS BIODETECTION AND BIOCONTROL TECHNOLOGY CO., LTD.·Registered Sep 11, 2013 – Sep 11, 2018Cancelled

Registration details

Analysis ID: 6c7e1ee3f1fa019a0edb4101fc234014
Customs Code: DHA09600198104

Company information

Manufacturer: HANGZHOU GENESIS BIODETECTION AND BIOCONTROL TECHNOLOGY CO., LTD.
Manufacturer Country: China
Authorized Representative: GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Adenovirus Serological Reagent (C.3020)".
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3020 腺病毒血清試劑
Import Information: Input;; Chinese goods

Dates and status

Registration Date: Sep 11, 2013
Expiry Date: Sep 11, 2018
Cancellation Date: May 19, 2022

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Torch" adenovirus test set (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6c7e1ee3f1fa019a0edb4101fc234014 and manufactured by HANGZHOU GENESIS BIODETECTION AND BIOCONTROL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD..

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