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Muto ‘s Stain Reagent Kits for Anatomic Pathology(Non-Sterile) - Taiwan Registration 9556fe9850755d485f0164e77d6a1a5e

Access comprehensive regulatory information for Muto ‘s Stain Reagent Kits for Anatomic Pathology(Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9556fe9850755d485f0164e77d6a1a5e and manufactured by MUTO PURE CHEMICALS CO., LTD.. The authorized representative in Taiwan is CHIN I PAO 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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9556fe9850755d485f0164e77d6a1a5e
Registration Details
Taiwan FDA Registration: 9556fe9850755d485f0164e77d6a1a5e
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Device Details

Muto ‘s Stain Reagent Kits for Anatomic Pathology(Non-Sterile)
TW: 武藤解剖病理染色試劑組(未滅菌)
Risk Class 1
MD

Registration Details

9556fe9850755d485f0164e77d6a1a5e

Ministry of Health Medical Device Import Registration No. 002283

DHA08400228302

Company Information

Product Details

Staining cells or tissues for pathological diagnosis.

B Hematology and pathology devices

B1850 Dyes and chemical solution dyes

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026