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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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8 records meeting your search criteria returned- Product Code: KPA Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
LEICA BIOSYSTEMS MELBOURNE PTY. LTD BOND-III AUTOMATED STAINER 01/28/2022
LEICA BIOSYSTEMS MELBOURNE PTY. LTD BOND-III AUTOMATED STAINER 01/28/2022
LEICA BIOSYSTEMS MELBOURNE PTY. LTD BOND-III AUTOMATED STAINER 07/02/2021
LEICA BIOSYSTEMS MELBOURNE PTY. LTD BOND-III AUTOMATED STAINER 07/02/2021
LEICA BIOSYSTEMS MELBOURNE PTY. LTD BOND-MAX AUTOMATED STAINER 01/08/2021
LEICA BIOSYSTEMS MELBOURNE PTY. LTD BOND-MAX 11/12/2020
LEICA BIOSYSTEMS MELBOURNE PTY. LTD BOND-MAX 11/10/2020
VENTANA MEDICAL SYSTEMS INC BENCHMARK ULTRA STAINER MODULE 05/22/2019
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