Taiwan FDA registration 9ba55aeee8857a42f7ee37d6550b1557

"Nainoende" Influenza Virus A&B Rapid Test Reagent (Unsterilized)

TW: "奈諾恩得" 流感病毒A&B快速檢驗試劑 (未滅菌)

Taiwan·Risk Class 1·NANOENTEK INC.·Registered Jan 05, 2016 – Jan 05, 2021Cancelled

Registration details

Analysis ID: 9ba55aeee8857a42f7ee37d6550b1557
Customs Code: DHA09401604505

Company information

Manufacturer: NANOENTEK INC.
Manufacturer Country: Korea, Republic of
Authorized Representative: JOLEX INTERNATIONAL 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: import

Dates and status

Registration Date: Jan 05, 2016
Expiry Date: Jan 05, 2021
Cancellation Date: Mar 04, 2022

Cancellation information

Status: Logged out
Reason: 自請註銷;;屆期未申請展延

About this record

Access comprehensive regulatory information for "Nainoende" Influenza Virus A&B 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 9ba55aeee8857a42f7ee37d6550b1557 and manufactured by NANOENTEK INC.. The authorized representative in Taiwan is JOLEX INTERNATIONAL CO., LTD..

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