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Siemens Healthineers Adds Muscle To Global Antibody Testing Effort, In Talks With Vaccine Developers

 
• By Phil Greenfield

The company now has US emergency use designation for its new SARS-CoV-2 test, which can run on its global installed base of 20,000 analyzers at a current capacity of 50 million tests per month.

COV2T
• Source: Siemens Healthineers

Siemens Healthineers AG announced on 1 June that the US Food and Drug Administration has granted emergency use authorization (EUA) for its laboratory test to detect the presence of SARS-CoV-2 antibodies in blood. The test was CE marked last week and the company also plans to apply for 510(k) clearance for the test in the US to ensure the test is still available once the EUA is revoked.

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