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"Etixi" hand jika hemostasis time measurement equipment (sterilization) - Taiwan Registration 2c5981be34632a3aa127932ba53c262d

Access comprehensive regulatory information for "Etixi" hand jika hemostasis time measurement equipment (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2c5981be34632a3aa127932ba53c262d and manufactured by Accriva Diagnostics Inc.. The authorized representative in Taiwan is BioChain 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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2c5981be34632a3aa127932ba53c262d
Registration Details
Taiwan FDA Registration: 2c5981be34632a3aa127932ba53c262d
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Device Details

"Etixi" hand jika hemostasis time measurement equipment (sterilization)
TW: ใ€่‰พๅธ่ฅฟใ€žๆ‰‹ๅ‰ๅกๆญข่ก€ๆ™‚้–“ๆธฌๅฎšๅ™จๆ(ๆป…่Œ)
Risk Class 1

Registration Details

2c5981be34632a3aa127932ba53c262d

DHA04401195704

Company Information

United States

Product Details

It is limited to the first level of identification scope of the "Bleeding Time Measurement Device (B.6100)" of the Measures for the Classification and Grading of Medical Devices.

B Hematology, pathology, and genetics

B.6100 Bleeding Time Measuring Apparatus

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Jul 18, 2012

Jul 18, 2027