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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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14 records meeting your search criteria returned- Product Code: KDQ Product Problem: Tear, Rip or Hole in Device Packaging Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
ATRIUM MEDICAL CORPORATION DRAINS OASIS SINGLE 03/31/2023
ATRIUM MEDICAL CORPORATION DRAINS OCEAN SINGLE 02/02/2021
TELEFLEX MEDICAL PE ADULT-PED WET LF 05/26/2020
TELEFLEX MEDICAL PE ADULT-PED WET LF 05/26/2020
DEROYAL INDUSTRIES, INC. 1500CC CANISTER KIT 03/11/2020
TELEFLEX MEDICAL PE ADULT-PED WET LF 6/CS 12/16/2019
TELEFLEX MEDICAL PE ADULT-PED DRY/ WET LF 07/10/2019
ATRIUM MEDICAL CORPORATION OCEAN DRAINS 04/19/2019
ATRIUM MEDICAL CORPORATION OCEAN DRAINS 04/16/2019
ATRIUM MEDICAL CORPORATION OCEAN DRAINS 04/16/2019
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