"Xianchong" blood bag vibrator (unsterilized)
Taiwan·Risk Class 1·CENTRON CORPORATION·Registered Aug 23, 2007 – Aug 23, 2022Cancelled- Analysis ID
- dde3ed4b04524f033ab0b80e5d1e550f
- Customs Code
- DHA04400610103
- Manufacturer
- CENTRON CORPORATION
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Y.H. BIOTEK CO., LTD.
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Blood Mixers and Blood Gravimetric Analysis Devices (B.9195)".
- 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
- Aug 23, 2007
- Expiry Date
- Aug 23, 2022
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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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 dde3ed4b04524f033ab0b80e5d1e550f 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.