Taiwan FDA registration 0d2cf3c819b4d25aead388d034b91b10

"Wonderfu" Influenza A/B Virus Rapid Test Reagent (Unsterilized)

TW: "萬德孚" A/B型流感病毒快速檢測試劑 (未滅菌)

Taiwan·Risk Class 1·WONDFO BIOTECH CO., LTD·Registered Feb 25, 2016 – Feb 25, 2021Cancelled

Registration details

Analysis ID: 0d2cf3c819b4d25aead388d034b91b10
Customs Code: DHA09600264506

Company information

Manufacturer: WONDFO BIOTECH CO., LTD
Manufacturer Country: China
Authorized Representative: LIKWANG INSTRUMENTS 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: Chinese goods;; input

Dates and status

Registration Date: Feb 25, 2016
Expiry Date: Feb 25, 2021
Cancellation Date: Oct 12, 2023

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Wonderfu" Influenza A/B Virus Rapid Test Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0d2cf3c819b4d25aead388d034b91b10 and manufactured by WONDFO BIOTECH CO., LTD. The authorized representative in Taiwan is LIKWANG INSTRUMENTS CO., LTD..

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