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"Ai Kuailu" Respiratory Fusion Cell Virus/A+B Influenza Rapid Test Kit (Unsterilized) - Taiwan Registration c7aabba4fa70aa365837b93dce29330c

Access comprehensive regulatory information for "Ai Kuailu" Respiratory Fusion Cell Virus/A+B Influenza Rapid Test Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c7aabba4fa70aa365837b93dce29330c and manufactured by ACRO BIOTECH. INC.. The authorized representative in Taiwan is Grand Marquis IVD 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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c7aabba4fa70aa365837b93dce29330c
Registration Details
Taiwan FDA Registration: c7aabba4fa70aa365837b93dce29330c
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Device Details

"Ai Kuailu" Respiratory Fusion Cell Virus/A+B Influenza Rapid Test Kit (Unsterilized)
TW: "่‰พๅฟซ้œฒ"ๅ‘ผๅธ้“่žๅˆ็ดฐ่ƒž็—…ๆฏ’/A+Bๅž‹ๆต่กŒๆ€งๆ„Ÿๅ†’ๅฟซ้€Ÿๆชข้ฉ—ๅฅ—็ต„ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

c7aabba4fa70aa365837b93dce29330c

DHA09401926202

Company Information

United States

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)" and "Respiratory Fusion Cell Virus Serum Reagent (C.3480)".

C Immunology and microbiology

C.3330 ๆตๆ„Ÿ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘;; C.3480 ๅ‘ผๅธ้“่žๅˆ็ดฐ่ƒž็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Jul 04, 2018

Jul 04, 2023