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“Boditech” Hemochroma PLUS - Taiwan Registration a95d7c67d0b3ace5c8892c4fd4f04ae2

Access comprehensive regulatory information for “Boditech” Hemochroma PLUS in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a95d7c67d0b3ace5c8892c4fd4f04ae2 and manufactured by Boditech Med Inc.. The authorized representative in Taiwan is Y.H. BIOTEK CO., LTD..

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a95d7c67d0b3ace5c8892c4fd4f04ae2
Registration Details
Taiwan FDA Registration: a95d7c67d0b3ace5c8892c4fd4f04ae2
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Device Details

“Boditech” Hemochroma PLUS
TW: "波狄塔克"血紅素測量系統
Risk Class 2
MD

Registration Details

a95d7c67d0b3ace5c8892c4fd4f04ae2

Ministry of Health Medical Device Import No. 033132

DHA05603313203

Company Information

Korea, Republic of

Product Details

This product is a portable in vitro diagnostic instrument used to measure the heme value in the blood.

B Hematology and pathology devices

B5620 Automated Heme Analysis System

Imported from abroad

Dates and Status

Jan 14, 2020

Jan 14, 2025