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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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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

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ManufacturerBrand NameDate Report Received
DATEX-OHMEDA, INC. AESPIRE 7900 02/09/2022
DATEX-OHMEDA, INC. AISYS CS2 02/08/2022
DATEX-OHMEDA, INC. AISYS CS2 02/02/2022
ACCUTRON, INC. DIGITAL ULTRA FLOWMETER 01/19/2022
DATEX-OHMEDA, INC. CARESTATION 650 01/17/2022
DATEX-OHMEDA, INC. AESTIVA 7900 01/12/2022
DATEX-OHMEDA, INC. AESPIRE 7100 01/11/2022
DATEX-OHMEDA, INC. AISYS CS2 12/31/2021
DATEX-OHMEDA, INC. AISYS CS2 12/28/2021
DATEX-OHMEDA, INC. AISYS CS2 12/20/2021
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