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Kiromi uric acid reagent - Taiwan Registration 5b86506edd1d95f2c15eda7e6146ee7b

Access comprehensive regulatory information for Kiromi uric acid reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5b86506edd1d95f2c15eda7e6146ee7b and manufactured by SYNERMED INTERNATIONAL INC.. The authorized representative in Taiwan is PUREBLOOD-TECH INTERNATIONAL CORP..

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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5b86506edd1d95f2c15eda7e6146ee7b
Registration Details
Taiwan FDA Registration: 5b86506edd1d95f2c15eda7e6146ee7b
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Device Details

Kiromi uric acid reagent
TW: ๅ–œๆจ‚็พŽๅฐฟ้…ธ่ฉฆๅŠ‘
Risk Class 1
Cancelled

Registration Details

5b86506edd1d95f2c15eda7e6146ee7b

DHA04400028802

Company Information

United States

Product Details

It is used to measure the level of uric acid in human serum or blood.

A Clinical chemistry and clinical toxicology

import

Dates and Status

Jul 29, 2005

Jul 29, 2010

Nov 26, 2012

Cancellation Information

Logged out

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