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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
SHANGHAI DRAEGER MEDICAL INSTRUMENT CO. FABIUS PLUS XL 11/10/2023
SHANGHAI DRAEGER MEDICAL INSTRUMENT CO. ATLAN A350/A350 XL CC 11/10/2023
DRÄGERWERK AG & CO. KGAA FABIUS PLUS 11/09/2023
DRÄGERWERK AG & CO. KGAA PERSEUS A500 11/08/2023
DRÄGERWERK AG & CO. KGAA FABIUS GS PREMIUM 11/03/2023
DRÄGERWERK AG & CO. KGAA FABIUS GS 11/02/2023
DRÄGERWERK AG & CO. KGAA FABIUS MRI 11/02/2023
SHANGHAI DRAEGER MEDICAL INSTRUMENT CO. FABIUS PLUS XL 10/26/2023
SHANGHAI DRAEGER MEDICAL INSTRUMENT CO. FABIUS PLUS XL 10/26/2023
DRÄGERWERK AG & CO. KGAA APOLLO 10/26/2023
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