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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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284 records meeting your search criteria returned- Product Code: MDB Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
BIOMERIEUX INC. BACT/ALERT FA PLUS 11/18/2020
BIOMERIEUX INC. BACT/ALERT FA PLUS 11/18/2020
BIOMERIEUX INC. BACT/ALERT FN PLUS 11/17/2020
BIOMERIEUX INC. BACT/ALERT PF PLUS (PLASTIC) 10/23/2020
BIOMERIEUX INC. BACT/ALERT FA PLUS 10/23/2020
BIOMERIEUX INC. BACT/ALERT SA (PLASTIC) 10/14/2020
BIOMERIEUX INC. BACT/ALERT SA (PLASTIC) 10/14/2020
BIOMÉRIEUX, INC. VIRTUO A UNIT 09/30/2020
BIOMERIEUX INC. BACT/ALERT SN (PLASTIC) 09/09/2020
BIOMERIEUX INC. BACT/ALERT PF PLUS (PLASTIC) 09/09/2020
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