Taiwan FDA registration 916850c65a31e8b51e6400c5484f1819

Ikon single-step rotavirus adenovirus 2-in-1 (fecal) antigen rapid test reagent

TW: 艾康單一步驟輪狀病毒腺病毒二合一(糞便)抗原快速檢測試劑

Taiwan·Risk Class 1·ACON BIOTECH (HANGZHOU) CO., LTD.·Registered Mar 26, 2010 – Mar 26, 2015Cancelled

Registration details

Analysis ID: 916850c65a31e8b51e6400c5484f1819
Customs Code: DHA04600089401

Company information

Manufacturer: ACON BIOTECH (HANGZHOU) CO., LTD.
Manufacturer Country: China
Authorized Representative: Ariel Health Inc

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: Chinese goods;; input

Dates and status

Registration Date: Mar 26, 2010
Expiry Date: Mar 26, 2015
Cancellation Date: Apr 25, 2018

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for Ikon single-step rotavirus adenovirus 2-in-1 (fecal) antigen rapid test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 916850c65a31e8b51e6400c5484f1819 and manufactured by ACON BIOTECH (HANGZHOU) CO., LTD.. The authorized representative in Taiwan is Ariel Health Inc.

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