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"Nainoende" Influenza Virus A&B Rapid Test Reagent (Unsterilized) - Taiwan Registration 9ba55aeee8857a42f7ee37d6550b1557

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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9ba55aeee8857a42f7ee37d6550b1557
Registration Details
Taiwan FDA Registration: 9ba55aeee8857a42f7ee37d6550b1557
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Device Details

"Nainoende" Influenza Virus A&B Rapid Test Reagent (Unsterilized)
TW: "ๅฅˆ่ซพๆฉๅพ—" ๆตๆ„Ÿ็—…ๆฏ’A&Bๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

9ba55aeee8857a42f7ee37d6550b1557

DHA09401604505

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".

C Immunology and microbiology

C.3330 ๆตๆ„Ÿ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Jan 05, 2016

Jan 05, 2021

Mar 04, 2022

Cancellation Information

Logged out

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