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“ACRO” fFN Rapid Test Cassette (Non-Sterile) - Taiwan Registration 0f6df15e59914e04e0aded2fb0dbeb4f

Access comprehensive regulatory information for “ACRO” fFN Rapid Test Cassette (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 0f6df15e59914e04e0aded2fb0dbeb4f 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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0f6df15e59914e04e0aded2fb0dbeb4f
Registration Details
Taiwan FDA Registration: 0f6df15e59914e04e0aded2fb0dbeb4f
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Device Details

“ACRO” fFN Rapid Test Cassette (Non-Sterile)
TW: “艾快露” 纖維黏連蛋白檢驗試劑 (未滅菌)
Risk Class 1
MD

Registration Details

0f6df15e59914e04e0aded2fb0dbeb4f

Ministry of Health Medical Device Import No. 019261

DHA09401926100

Company Information

United States

Product Details

Limited to the first level identification range of the human growth hormone test system (A.1370) of the management measures for medical equipment.

A Clinical chemistry and clinical toxicology

A1370 Human Growth Hormone Test System

Imported from abroad

Dates and Status

Jul 04, 2018

Jul 04, 2023