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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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166 records meeting your search criteria returned- Product Code: BTM Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
AMBU A/S SPUR® II ADULT RESUSCITATORSINGLE PATIEN 01/16/2020
SUNMED HOLDINGS, LLC. MEDLINE 01/06/2020
SUNMED HOLDINGS LLC. AIRFLOW 12/05/2019
SUNMED HOLDINGS LLC. SAFESPOT 11/05/2019
MERCURY ENTERPRISES, INC. INFANT CPR BAG 10/07/2019
SUNMED HOLDINGS LLC. AIRFLOW 10/04/2019
SUNMED HOLDINGS, LLC. AIRFLOW 09/27/2019
SUNMED HOLDINGS LLC. AIRFLOW 09/26/2019
SUNMED HOLDINGS, LLC. AIRFLOW 09/03/2019
SUNMED HOLDINGS LLC. AIRFLOW 08/27/2019
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