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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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70 records meeting your search criteria returned- Product Code: LQL Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
BIOMERIEUX INC. VITEK® 2 GRAM POSITIVE ID TEST KIT 05/02/2018
BIOMERIEUX INC. VITEK® 2 GRAM POSITIVE ID TEST KIT 03/09/2018
BIOMÉRIEUX, INC. VITEK® 2 GRAM-POSITIVE (GP) IDENTIFICATI 02/22/2018
BIOMERIEUX, INC VITEK® 2 GP TEST KIT 01/30/2018
BIOMERIEUX INC. VITEK® 2 GRAM POSITIVE IDENTIFICATION TE 01/24/2018
BIOMERIEUX, INC VITEK® 2 GP TEST KIT 11/14/2017
BIOMERIEUX INC. VITEK® 2 GRAM POSITIVE TEST KIT 10/10/2017
BIOMERIEUX, INC VITEK® 2 GRAM-POSITIVE IDENTIFICATION TE 06/22/2017
BIOMERIEUX, INC VITEK® 2 GRAM-POSITIVE (GP) IDENTIFICATI 06/06/2017
BIOMERIEUX, INC VITEK® 2 GP TEST KIT 04/27/2017
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