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Fukushima Quick-take Streptococcus B Rapid Assay Reagent - Taiwan Registration d92bba0b36cc16cbf50e930b313f7972

Access comprehensive regulatory information for Fukushima Quick-take Streptococcus B Rapid Assay Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d92bba0b36cc16cbf50e930b313f7972 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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d92bba0b36cc16cbf50e930b313f7972
Registration Details
Taiwan FDA Registration: d92bba0b36cc16cbf50e930b313f7972
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Device Details

Fukushima Quick-take Streptococcus B Rapid Assay Reagent
TW: ็ฆๅณถๅฟซๅ–้ˆ็ƒ่ŒB็พคๅฟซ้€Ÿๆธฌๅฎš่ฉฆๅŠ‘
Risk Class 1
Cancelled

Registration Details

d92bba0b36cc16cbf50e930b313f7972

DHA04400230308

Company Information

France

Product Details

Qualitative detection of group B streptococcal antigen in human vaginal specimens.

C Immunology and microbiology

C.3740 ้ˆ็ƒ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Dec 22, 2005

Dec 22, 2010

Nov 20, 2012

Cancellation Information

Logged out

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