Taiwan FDA registration b130d8f956d7579a14c116f9c8420b29
Lendo corrected serum
TW: 倫多校正血清
Taiwan·Risk Class 2·RANDOX LABORATORIES LTD·Registered Feb 17, 2006 – Feb 17, 2011CancelledRegistration details
- Analysis ID
- b130d8f956d7579a14c116f9c8420b29
- Customs Code
- DHA00601600802
Company information
- Manufacturer
- RANDOX LABORATORIES LTD
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EUGENE-CHEN CO., LTD.
Product details
- Intended Use
- It is used as a corrector in clinical biochemical analysis.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- import
Dates and status
- Registration Date
- Feb 17, 2006
- Expiry Date
- Feb 17, 2011
- Cancellation Date
- Oct 13, 2011
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Lendo corrected serum in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b130d8f956d7579a14c116f9c8420b29 and manufactured by RANDOX LABORATORIES LTD. The authorized representative in Taiwan is EUGENE-CHEN CO., LTD..
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