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"Aikuailu" Respiratory Fusion Cell Virus Rapid Test Reagent (Unsterilized) - Taiwan Registration 9de758cf7b69c35d5e271b0e466ece9a

Access comprehensive regulatory information for "Aikuailu" Respiratory Fusion Cell 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 9de758cf7b69c35d5e271b0e466ece9a 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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9de758cf7b69c35d5e271b0e466ece9a
Registration Details
Taiwan FDA Registration: 9de758cf7b69c35d5e271b0e466ece9a
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Device Details

"Aikuailu" Respiratory Fusion Cell Virus Rapid Test Reagent (Unsterilized)
TW: "่‰พๅฟซ้œฒ" ๅ‘ผๅธ้“่žๅˆ็ดฐ่ƒž็—…ๆฏ’ๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

9de758cf7b69c35d5e271b0e466ece9a

DHA09401699109

Company Information

United States

Product Details

Limited to the classification and grading management of medical devices, the first level identification range of "respiratory fusion cell virus serum reagent (C.3480)".

C Immunology and microbiology

C.3480 ๅ‘ผๅธ้“่žๅˆ็ดฐ่ƒž็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

Input;; QMS/QSD

Dates and Status

Sep 10, 2016

Sep 10, 2026