Taiwan FDA registration e40dd746fc416f394bb8a62812497b06

Wonderford influenza A virus rapid detection reagent

TW: 萬德福A型流感病毒快速檢測試劑

Taiwan·Risk Class 1·WONDFO BIOTECH CO., LTD·Registered Sep 30, 2009 – Sep 30, 2014Cancelled

Registration details

Analysis ID: e40dd746fc416f394bb8a62812497b06
Customs Code: DHA04600080206

Company information

Manufacturer: WONDFO BIOTECH CO., LTD
Manufacturer Country: China
Authorized Representative: GENERAL BIOLOGICALS CORP.

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: Chinese goods;; input

Dates and status

Registration Date: Sep 30, 2009
Expiry Date: Sep 30, 2014
Cancellation Date: Jun 28, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Wonderford influenza A virus rapid detection reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e40dd746fc416f394bb8a62812497b06 and manufactured by WONDFO BIOTECH CO., LTD. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..

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