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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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125 records meeting your search criteria returned- Product Code: OMP Product Problem: Overheating of Device Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
SMITH & NEPHEW MEDICAL LTD. RENASYS TOUCH NON CONNECT 4TH ED DEVICE 07/23/2020
CARDINAL HEALTH NPWT FACILITY NPWT SVED THERAPY DEVICE 07/14/2020
CARDINAL HEALTH NPWT FACILITY NPWT SVED THERAPY DEVICE 07/07/2020
KINETIC CONCEPTS, INC. V.A.C. FREEDOM THERAPY SYSTEM 06/11/2020
SMITH & NEPHEW MEDICAL LTD. RENASYS GO 05/07/2020
SMITH & NEPHEW MEDICAL LTD. RENASYS TOUCH DEVICE & POWER SUP 04/23/2020
CARDINAL HEALTH NPWT FACILITY NPWT SVED THERAPY DEVICE 04/09/2020
SMITH & NEPHEW MEDICAL LTD. RENASYS GO 03/27/2020
SMITH & NEPHEW MEDICAL LTD. RENASYS TOUCH DEVICE & POWER SUP 02/06/2020
SMITH & NEPHEW MEDICAL LTD. RENASYS GO 01/22/2020
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