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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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253 records meeting your search criteria returned- Product Code: KDJ Product Problem: Unsealed Device Packaging Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
BAXTER HEALTHCARE CORPORATION MINICAP TRANSFER SET 03/18/2024
BAXTER HEALTHCARE CORPORATION MINICAP 02/12/2024
BAXTER HEALTHCARE CORPORATION MINICAP TRANSFER SET 02/05/2024
BAXTER HEALTHCARE CORPORATION MINICAP TRANSFER SET 12/19/2023
BAXTER HEALTHCARE CORPORATION MINICAP TRANSFER SET 12/12/2023
BAXTER HEALTHCARE CORPORATION MINICAP TRANSFER SET 12/12/2023
BAXTER HEALTHCARE CORPORATION MINICAP TRANSFER SET 11/01/2023
BAXTER HEALTHCARE CORPORATION MINICAP 10/03/2023
BAXTER HEALTHCARE CORPORATION MINICAP TRANSFER SET 09/29/2023
BAXTER HEALTHCARE CORPORATION MINICAP 09/28/2023
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