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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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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

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ManufacturerBrand NameDate Report Received
Unknown Manufacturer SHUNT 12/13/2021
Unknown Manufacturer SHUNT 12/13/2021
MEDTRONIC NEUROSURGERY MEDTRONIC STRATA SHUNT 12/13/2021
MEDTRONIC NEUROSURGERY STRATA 12/13/2021
MEDTRONIC NEUROSURGERY UNKNOWN VALVE/SHUNT 12/13/2021
CHRISTOPH MIETHKE GMBH & CO KG PROGAV WITH SHUNTASSISTANT 20 12/13/2021
CHRISTOPH MIETHKE GMBH & CO KG PROGAV SYS W/SA 20 A.CONTROL RESERVOIR 12/13/2021
CHRISTOPH MIETHKE GMBH & CO KG PROGAV SYS PED.W/SA 20 A.PRECHAMBER 12/13/2021
CHRISTOPH MIETHKE GMBH & CO KG PROGAV SYS W/SA 20 A.CONTROL RESERVOIR 12/13/2021
CHRISTOPH MIETHKE GMBH & CO KG GAV W.DISTAL CATH.10/40 12/13/2021
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