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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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6 records meeting your search criteria returned- Product Code: DPS Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
GE MEDICAL SYSTEMS INFORMATION TECHNOLOG EKG, MULTI CHANNEL, INTERPRETATIVE - GE 01/07/2022
MIDMARK CORPORATION MIDMARK IQECG 10/27/2020
MIDMARK CORPORATION IQECG 07/17/2019
PHILIPS MEDICAL SYSTEMS PAGEWRITER TOUCH CARDIOGRAPH 01/06/2017
PHILIPS MEDICAL SYSTEMS PAGEWRITER TC30 CARDIOGRAPH 12/23/2015
PHILIPS MEDICAL SYSTEMS PAGEWRITER TRIM III CARDIOGRAPH 06/10/2014
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