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"Echoroll" Respiratory Fusion Virus Test Reagent (Non-sterile) - Taiwan Registration b4c151159b0b5b40fdc3bc82b1d358aa

Access comprehensive regulatory information for "Echoroll" Respiratory Fusion Virus Test Reagent (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b4c151159b0b5b40fdc3bc82b1d358aa and manufactured by ACRO BIOTECH. INC.. The authorized representative in Taiwan is APPLIED BIOTECH ENTERPRISE 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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b4c151159b0b5b40fdc3bc82b1d358aa
Registration Details
Taiwan FDA Registration: b4c151159b0b5b40fdc3bc82b1d358aa
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Device Details

"Echoroll" Respiratory Fusion Virus Test Reagent (Non-sterile)
TW: "ๆ„›ๅฏ็พ…" ๅ‘ผๅธ้“่žๅˆ็—…ๆฏ’ๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

b4c151159b0b5b40fdc3bc82b1d358aa

DHA09402329101

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

Oct 27, 2023

Oct 27, 2028