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Kiromi alkaline phosphatase reagent - Taiwan Registration 6b48d09cd3d05809a8b2caae5d3dc295

Access comprehensive regulatory information for Kiromi alkaline phosphatase reagent in Taiwan's medical device market through Pure Global AI's free database. is registered under number 6b48d09cd3d05809a8b2caae5d3dc295 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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6b48d09cd3d05809a8b2caae5d3dc295
Registration Details
Taiwan FDA Registration: 6b48d09cd3d05809a8b2caae5d3dc295
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Device Details

Kiromi alkaline phosphatase reagent
TW: ๅ–œๆจ‚็พŽ้นผๆ€ง็ฃท้…ธ้…ถ่ฉฆๅŠ‘
Cancelled

Registration Details

6b48d09cd3d05809a8b2caae5d3dc295

DHA00601325402

Company Information

United States

Product Details

Quantify the amount of frenetic phosphatase in human serum.

A Clinical chemistry and clinical toxicology

import

Dates and Status

Oct 26, 2005

Oct 26, 2010

Nov 26, 2012

Cancellation Information

Logged out

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