"Xianchong" blood bag vibrator (unsterilized)
- Analysis ID
- d9f875e8877fe57e1983a17770b9dfd7
- Customs Code
- DHA08400610100
- Manufacturer
- CENTRON CORPORATION
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Y.H. BIOTEK CO., LTD.
- 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
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
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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.