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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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2 records meeting your search criteria returned- Product Code: KGG Patient Problem: Nerve Damage Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
MEDOS INTERNATIONAL SARL TRUFILL N-BCA-1 GRAM KIT 01/05/2023
MEDOS INTERNATIONAL SARL UNK LIQUID EMBOLIC 10/12/2021
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