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Fukushima Rapid Prostate-Specific Antigen Assay Reagent - Taiwan Registration a58fcefda4bb0ed8a520a3c089eeccae

Access comprehensive regulatory information for Fukushima Rapid Prostate-Specific Antigen Assay Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a58fcefda4bb0ed8a520a3c089eeccae and manufactured by VEDA LAB. The authorized representative in Taiwan is Fukushima Medical Equipment 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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a58fcefda4bb0ed8a520a3c089eeccae
Registration Details
Taiwan FDA Registration: a58fcefda4bb0ed8a520a3c089eeccae
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Device Details

Fukushima Rapid Prostate-Specific Antigen Assay Reagent
TW: ็ฆๅณถๅฟซๅ–ๅ‰ๅˆ—่…บ็‰น็•ฐๆŠ—ๅŽŸๅฟซ้€Ÿๆธฌๅฎš่ฉฆๅŠ‘
Risk Class 2
Cancelled

Registration Details

a58fcefda4bb0ed8a520a3c089eeccae

DHA00601638503

Company Information

France

Product Details

Qualitative detection of prostate-specific antigen (PSA) in human whole blood, plasma and serum.

C Immunology and microbiology

C.6010 ่…ซ็˜ค็›ธ้—œๆŠ—ๅŽŸๅ…็–ซ่ฉฆ้ฉ—็ณป็ตฑ

import

Dates and Status

Apr 19, 2006

Apr 19, 2011

Nov 20, 2012

Cancellation Information

Logged out

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