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"Probiotic" pylori reagents - Taiwan Registration 76eea1b73ced174c2335723bc4bd9e75

Access comprehensive regulatory information for "Probiotic" pylori reagents in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 76eea1b73ced174c2335723bc4bd9e75 and manufactured by MD BIOTECH CORPORATION. The authorized representative in Taiwan is Yisheng Technology Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MD BIOTECH CORPORATION, and 1 recent registrations in the same category. 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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76eea1b73ced174c2335723bc4bd9e75
Registration Details
Taiwan FDA Registration: 76eea1b73ced174c2335723bc4bd9e75
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Device Details

"Probiotic" pylori reagents
TW: "็›Š็”Ÿ"ๅนฝ้–€ๆกฟ่Œ่ฉฆๅŠ‘
Risk Class 1
Cancelled

Registration Details

76eea1b73ced174c2335723bc4bd9e75

DHA04400293506

Company Information

United States

Product Details

Rapid identification of urea content of Helicobacter pylori in samples.

C Immunology and microbiology

C.0003 ่žบๆ—‹ๆกฟ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Mar 14, 2006

Mar 14, 2016

Apr 25, 2018

Cancellation Information

Logged out

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