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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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337 records meeting your search criteria returned- Product Code: CBK Product Problem: Device Sensing Problem Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
MEDTRONIC / COVIDIEN MEDTRONIC 980 BENNETT 10/03/2022
RESMED LTD ASTRAL 150 DBL KIT FRA 06/16/2022
IMTMEDICAL AG BELLAVISTA 06/08/2022
RESPIRONICS INC. Sensor 12/21/2021
DRAEGERWERK AG & CO. KGAA V500 12/16/2021
RESMED LTD ASTRAL 150 DBL KIT FRA 12/14/2021
NEWPORT MEDICAL INSTRUMENT, INC. H70 VENTILATOR 11/22/2021
RESMED LTD ASTRAL 150 - AMER 11/03/2021
RESMED PTY LTD ASTRAL 150 VENTILATOR 10/29/2021
IMTMEDICAL AG BELLAVISTA 08/19/2021
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