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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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93 records meeting your search criteria returned- Product Code: DQY Product Problem: Migration or Expulsion of Device Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
ARROW INTERNATIONAL INC., / SUBSIDIARY O ARROW INTERNATIONAL TELEFLEX KIT AK-2124 04/16/2019
COVIDIEN CHOCOLATE 07/27/2018
MICRO THERAPEUTICS, INC. D/B/A EV3 NEURO SUPPORT GUIDECATHETER 07/26/2018
ASAHI INTECC CO., LTD. ASAHI CARAVEL MICROCATHETER 135 CM 07/13/2018
ARROW INTERNATIONAL INC. ARROW CVC SET: 2-LUMEN 4 FR X 8 CM 05/15/2018
ARROW INTERNATIONAL INC. ARROW CVC SET: 5-LUMEN 9.5FR X 20CM 03/22/2018
ARROW INTERNATIONAL INC. ARROW CVC SET: 5-LUMEN 9.5FR X 20CM 03/22/2018
ARROW INTERNATIONAL INC. ARROW CVC SET: 3-LUMEN 7FR X 20CM 02/08/2018
PENUMBRA, INC. NEURON MAX 6F 088 LONG SHEATH 02/02/2018
PENUMBRA NEURON MAX 088 01/11/2018
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