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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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379 records meeting your search criteria returned- Product Code: DRY Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO CDI BLOOD PARAMETER MONITORING SYSTEM 55 01/11/2021
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO CDI BLOOD PARAMETER MONITORING SYSTEM 55 01/11/2021
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO CDI BLOOD PARAMETER MONITORING SYSTEM 50 01/04/2021
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO CDI BLOOD PARAMETER MONITORING SYSTEM 55 12/22/2020
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO CDI BLOOD PARAMETER MONITORING SYSTEM 55 12/22/2020
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO CDI BLOOD PARAMETER MONITORING SYSTEM 50 12/21/2020
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO CDI BLOOD PARAMETER MONITORING SYSTEM 55 10/21/2020
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO CDI BLOOD PARAMETER MONITORING SYSTEM 55 10/21/2020
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO CDI BLOOD PARAMETER MONITORING SYSTEM 55 10/21/2020
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO CDI BLOOD PARAMETER MONITORING SYSTEM 50 08/28/2020
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