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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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81 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
INVACARE REHABILITATION EQUIP NON AC-POWERED PATIENT LIFT 10/13/2014
ARJOHUNTLEIGH MAGOG INC. MAXI 500 09/18/2014
VANCARE, INC. VANDERLIFT 08/27/2014
INVACARE REHABILITATION EQUIP NON AC-POWERED PATIENT LIFT 08/21/2014
Unknown Manufacturer MEDIUM MULTI-PURPOSE SLING, KNIT STYLE 07/14/2014
LIKO AB LIKORAIL 242 S 07/10/2014
INVAMEX NON AC-POWERED PATIENT LIFT 06/19/2014
MEDLINE INDUSTRIES, INC. PATIENT LIFT 06/13/2014
ARJOHUNTLEIGH POLSKA SP. ZO.O. MIRANTI 04/29/2014
ARJO HUNTLEIGH POLSKA SP. Z.O.O. MIRANTI 04/29/2014
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