Taiwan FDA registration d9f875e8877fe57e1983a17770b9dfd7

"Xianchong" blood bag vibrator (unsterilized)

TW: "先崇"血袋振盪器(未滅菌)
Taiwan flagTaiwan·Risk Class 1·CENTRON CORPORATION·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
d9f875e8877fe57e1983a17770b9dfd7
Customs Code
DHA08400610100
Company information
Manufacturer Country
Korea, Republic of
Authorized Representative
Y.H. BIOTEK CO., LTD.
Product details
Intended Use
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.
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.9195 Blood Mixers and Blood Gravimetric Analysis Devices
Import Information
import
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
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About this record

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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