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Firstep Respiratory Syncytial Virus(RSV) Rapid Test (Non-Sterile) - Taiwan Registration b2bbf342ba56424a330c07921dd5bd60

Access comprehensive regulatory information for Firstep Respiratory Syncytial Virus(RSV) Rapid Test (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 b2bbf342ba56424a330c07921dd5bd60 and manufactured by FIRSTEP BIORESEARCH INC.. The authorized representative in Taiwan is FIRSTEP BIORESEARCH INC..

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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b2bbf342ba56424a330c07921dd5bd60
Registration Details
Taiwan FDA Registration: b2bbf342ba56424a330c07921dd5bd60
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Device Details

Firstep Respiratory Syncytial Virus(RSV) Rapid Test (Non-Sterile)
TW: ่ฏ่ฏๅ‘ผๅธ้“่žๅˆ็ดฐ่ƒž็—…ๆฏ’ๆชขๆธฌ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

b2bbf342ba56424a330c07921dd5bd60

Ministry of Health Medical Device Manufacturing No. 007851

Company Information

Taiwan, Province of China

Product Details

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

C Immunology and microbiology devices

C3480 Respiratory Fusion Cell Virus Serological Reagent

Produced in Taiwan, China

Dates and Status

Jul 12, 2019

Jul 12, 2024