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RAMP NT-proBNP Assay - Taiwan Registration 5ffd8356937121f4d7f0759105097134

Access comprehensive regulatory information for RAMP NT-proBNP Assay in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5ffd8356937121f4d7f0759105097134 and manufactured by RESPONSE BIOMEDICAL CORPORATION. The authorized representative in Taiwan is RECHI CO., LTD..

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5ffd8356937121f4d7f0759105097134
Registration Details
Taiwan FDA Registration: 5ffd8356937121f4d7f0759105097134
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Device Details

RAMP NT-proBNP Assay
TW: โ€œๅ€ซๆ™ฎโ€N็ซฏๅ‰Bๅž‹ๅˆฉ้ˆ‰่‚ฝๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 2
MD

Registration Details

5ffd8356937121f4d7f0759105097134

Ministry of Health Medical Device Import No. 027561

DHA05602756101

Company Information

Product Details

With RAMP Reader System or RAMP 200 System, immunochromography, the concentration of NT-proBNP in EDTA whole blood was quantitatively detected.

A Clinical chemistry and clinical toxicology

A1117 Type B sodium urine peptide test system

Imported from abroad

Dates and Status

Aug 26, 2015

Aug 26, 2025