Taiwan FDA registration e52e353ea11232e6515388512b732435
"Xianchong" plasma platen
TW: “先崇”血漿壓板
Taiwan·Risk Class 1·CENTRON TECHNOLOGIES CORPORATION·Registered Apr 18, 2006 – Apr 18, 2011CancelledRegistration details
- Analysis ID
- e52e353ea11232e6515388512b732435
- Customs Code
- DHA04400400905
Company information
- Manufacturer
- CENTRON TECHNOLOGIES CORPORATION
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Y.H. BIOTEK CO., LTD.
Product details
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9050 Blood bank supply equipment
- Import Information
- import
Dates and status
- Registration Date
- Apr 18, 2006
- Expiry Date
- Apr 18, 2011
- Cancellation Date
- Oct 26, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Xianchong" plasma platen in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e52e353ea11232e6515388512b732435 and manufactured by CENTRON TECHNOLOGIES CORPORATION. The authorized representative in Taiwan is Y.H. BIOTEK CO., LTD..
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