Taiwan FDA registration 51fd92eddc1672fcfce1c8a89aa9ac16

"Dongyao" Influenza A/B Rapid Test Set (Unsterilized)

TW: "東耀" 流感A/B型快速檢測試劑組 (未滅菌)

Taiwan·Risk Class 1·TONYAR BIOTECH. INC.·Registered Aug 10, 2016 – Aug 10, 2021Cancelled

Registration details

Analysis ID: 51fd92eddc1672fcfce1c8a89aa9ac16

Company information

Manufacturer: TONYAR BIOTECH. INC.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: TONYAR BIOTECH. INC.

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 10, 2016
Expiry Date: Aug 10, 2021
Cancellation Date: Aug 28, 2023

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Dongyao" Influenza A/B Rapid 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 51fd92eddc1672fcfce1c8a89aa9ac16 and manufactured by TONYAR BIOTECH. INC.. The authorized representative in Taiwan is TONYAR BIOTECH. INC..

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