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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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173 records meeting your search criteria returned- Product Code: MUQ Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
ARTIVION, INC. BIOGLUE SYRINGE 5-PACK, 5ML, G 03/13/2024
ARTIVION, INC. BIOGLUE SYRINGE 5-PACK, 5ML, G 02/27/2024
ARTIVION, INC. BIOGLUE SYRINGE 5-PACK, 10 ML, JAPAN 03/29/2023
ARTIVION, INC. BIOGLUE SYRINGE 5-PACK, 10 ML,JAPAN 03/29/2023
ARTIVION, INC. BIOGLUE - UNKNOWN CONFIGURATION 03/02/2023
ARTIVION, INC. ¿ KENNESAW BIOGLUE - UNKNOWN CONFIGURATION 11/24/2022
ARTIVION, INC. BIOGLUE - UNKNOWN CONFIGURATION 11/02/2022
ARTIVION, INC. 2022-3718 11/02/2022
ARTIVION, INC. BIOGLUE - UNKNOWN CONFIGURATION 10/04/2022
ARTIVION, INC. BIOGLUE SYRINGE 5-PACK, 2ML 09/30/2022
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