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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
GE MEDICAL SYSTEMS (CHINA) CO., LTD (WUX CARESTATION 650 07/11/2023
DATEX-OHMEDA INC AVANCE 02/01/2022
DATEX-OHMEDA, INC. AVANCE CS2 08/20/2020
GE HEALTHCARE/ DATEX-OHMEDA, INC. GE HEALTHCARE AISYS CS2 ANESTHESIA MACHI 06/05/2020
DRÄGERWERK AG & CO. KGAA FABIUS PLUS 10/02/2019
DRÄGERWERK AG & CO. KGAA FABIUS GS 10/01/2019
DATEX-OHMEDA, INC. AVANCE CS2 09/30/2019
DRÄGERWERK AG & CO. KGAA FABIUS GS PREMIUM 09/02/2019
DRÄGERWERK AG & CO. KGAA PRIMUS 08/15/2019
DRÄGERWERK AG & CO. KGAA PERSEUS A500 07/18/2019
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