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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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135 records meeting your search criteria returned- Product Code: NBW Product Problem: Unsealed Device Packaging Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
LIFESCAN EUROPE, A DIVISION OF CILAG GMB OT VERIO TEST STRIPS 02/01/2017
ASCENSIA DIABETES CARE US INC. CONTOUR 01/26/2017
ASCENSIA DIABETES CARE US INC. CONTOUR NEXT 01/25/2017
LIFESCAN EUROPE, A DIVISION OF CILAG GMB OT VERIO TEST STRIPS 12/15/2016
LIFESCAN EUROPE, A DIVISION OF CILAG GMB OT VERIO TEST STRIPS 12/06/2016
LIFESCAN EUROPE, A DIVISION OF CILAG GMB OT VERIO FLEX METER 12/02/2016
LIFESCAN EUROPE, A DIVISION OF CILAG GMB OT VERIO FLEX METER 11/29/2016
LIFESCAN EUROPE, A DIVISION OF CILAG GMB OT VERIO TEST STRIPS 11/18/2016
LIFESCAN EUROPE, A DIVISION OF CILAG GMB OT VERIO TEST STRIPS 10/28/2016
LIFESCAN EUROPE, A DIVISION OF CILAG GMB OT VERIO2 METER 10/27/2016
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