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"Xianchong" blood bag vibrator (unsterilized) - Taiwan Registration d9f875e8877fe57e1983a17770b9dfd7

Access comprehensive regulatory information for "Xianchong" blood bag vibrator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d9f875e8877fe57e1983a17770b9dfd7 and manufactured by CENTRON CORPORATION. The authorized representative in Taiwan is Y.H. BIOTEK CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CENTRON CORPORATION, and 1 recent registrations in the same category. 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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d9f875e8877fe57e1983a17770b9dfd7
Registration Details
Taiwan FDA Registration: d9f875e8877fe57e1983a17770b9dfd7
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Device Details

"Xianchong" blood bag vibrator (unsterilized)
TW: "ๅ…ˆๅด‡"่ก€่ข‹ๆŒฏ็›ชๅ™จ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

d9f875e8877fe57e1983a17770b9dfd7

DHA08400610100

Company Information

Korea, Republic of

Product Details

It is limited to the first level of identification of the "Blood Mixer and Blood Gravimetric Analysis Device (B.9195)" of the Administrative Measures for the Classification and Grading of Medical Devices.

B Hematology, pathology, and genetics

B.9195 Blood Mixers and Blood Gravimetric Analysis Devices

import

Dates and Status

Oct 01, 2021

Oct 31, 2025

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