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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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138 records meeting your search criteria returned- Product Code: KDQ Product Problem: Fluid/Blood Leak Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
TELEFLEX MEDICAL PE ADULT-PED DRY/ WET LF 11/18/2020
TELEFLEX MEDICAL PE ADULT-PED DRY/ WET LF 11/05/2020
TELEFLEX MEDICAL PE ADULT-PED DRY/ WET LF 09/08/2020
TELEFLEX MEDICAL PE ADULT-PED DRY/ WET LF 09/08/2020
TELEFLEX MEDICAL PE ADULT-PED DRY/ WET LF 08/10/2020
ATRIUM MEDICAL CORPORATION DRAINS PNEUMOSTAT 08/06/2020
TELEFLEX MEDICAL PE ADULT-PED DRY/ WET LF 08/05/2020
TELEFLEX MEDICAL PE ADULT-PED DRY/ WET LF 07/23/2020
TELEFLEX MEDICAL PE SAHARA DRY SUCT/DRY SEAL LF 6/CS 06/08/2020
ATRIUM MEDICAL CORPORATION OCEAN SINGLE DRAIN 03/22/2020
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