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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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80 records meeting your search criteria returned- Product Code: FSA Product Problem: Improper or Incorrect Procedure or Method Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
PRISM MEDICAL CEILING MOUNTED PATIENT LIFT 09/14/2017
ARJOHUNTLEIGH POLSKA SP. Z O.O. TENOR 08/26/2016
ARJOHUNTLEIGH POLSKA SP. Z O.O. SARA 3000 08/01/2016
GULDMANN INC. GULDMANN REPOSITIONIN SLING 07/22/2016
JOERNS HEALTHCARE HOYER HPL500 06/29/2016
HANDI-MOVE HANDI MOVE 2510 CEILING MOTOR 06/28/2016
UNKNOWN RELIANT 450 POWER LOW BASE LIFT 91536467 06/21/2016
INVAMEX POWER LIFT W/LOW BASE-PLUS 9153633519 05/25/2016
INVAMEX POWER LIFT W/LOW BASE-PLUS 9153633519 05/04/2016
LIKO AB GOLVO 7007 ES 04/05/2016
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