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Reagent for Mitsubishi urea nitrogen determination - Taiwan Registration 28f41bafddcd2c30c5d4c7df1b7f4733

Access comprehensive regulatory information for Reagent for Mitsubishi urea nitrogen determination in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 28f41bafddcd2c30c5d4c7df1b7f4733 and manufactured by MITSUBISHI KAGAKU IATRON. INC.. The authorized representative in Taiwan is Jingxiang 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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28f41bafddcd2c30c5d4c7df1b7f4733
Registration Details
Taiwan FDA Registration: 28f41bafddcd2c30c5d4c7df1b7f4733
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Device Details

Reagent for Mitsubishi urea nitrogen determination
TW: ไธ‰่ฑๅฐฟ็ด ๆฐฎๆธฌๅฎš็”จ่ฉฆๅŠ‘
Risk Class 2
Cancelled

Registration Details

28f41bafddcd2c30c5d4c7df1b7f4733

DHA00601718908

Company Information

Product Details

Measure urea nitrogen in human serum, blood and urine.

A Clinical chemistry and clinical toxicology

A.1770 ๅฐฟ็ด ๆฐฎ่ฉฆ้ฉ—็ณป็ตฑ

import

Dates and Status

Jul 04, 2006

Jul 04, 2011

Oct 30, 2012

Cancellation Information

Logged out

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