Sanmeng corrected reference serum
Taiwan·Risk Class 2·FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A SUBSIDIARY OF THERMO FISHER·Registered Dec 11, 2009 – Dec 11, 2014Cancelled- Analysis ID
- 60370cc7ed8482dc1c2cfa70b8492980
- Customs Code
- DHA00602073700
- Manufacturer
- FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A SUBSIDIARY OF THERMO FISHER
- Manufacturer Country
- United States
- Authorized Representative
- BEAM INTERNATIONAL INC.
- Intended Use
- This calibration serum is used on clinical chemistry analyzers as a secondary calibrator for general analysis
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- import
- Registration Date
- Dec 11, 2009
- Expiry Date
- Dec 11, 2014
- Cancellation Date
- May 17, 2018
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for Sanmeng corrected reference serum in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 60370cc7ed8482dc1c2cfa70b8492980 and manufactured by FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A SUBSIDIARY OF THERMO FISHER. The authorized representative in Taiwan is BEAM INTERNATIONAL INC..
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