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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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220 records meeting your search criteria returned- Product Code: DTZ Product Problem: Use of Device Problem Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX25RWC W/ RES 05/19/2021
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX25REC W/RES 04/23/2021
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO HOLLOW FIBER OXY WITH 4000 ML 03/10/2021
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX25RWC W/ RES 03/05/2021
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX25RWC W/ RES 02/22/2021
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO NS FX25REC W/RES 12/24/2020
PERFUSION SYSTEMS AFFINITY HFO W/TRILLIUM 511T 12/22/2020
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO NS FX25REC W/RES 12/21/2020
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO NS FX25REC W/RES 12/21/2020
PERFUSION SYSTEMS AFFINITY HFO W/TRILLIUM 511T 11/25/2020
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