12 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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TENODESIS CROSS SCREW, INTERFERENCE SCREW, SUTURE BEAD
FDA 510(k)
FDA Class 2
·Orthopedic
SchureMed
FDA UDI
SCHUERCH CORPORATION·00810057371264·SCHURE SPINE PAD SET (SOFC W/GEL)
PHASE II GBM IGG ANTIBODY EIA TEST
FDA 510(k)
FDA Class 2
·Immunology
ST/AR ST AND ARRHYTHMIA SOFTWARE
FDA 510(k)
FDA Class 2
·Cardiovascular
CARTIVA IMPLANT
FDA Adverse Event
Injury
·CARTIVA, INC·Product code PNW·November 13, 2020
CARTIVA IMPLANT
FDA Adverse Event
Injury
·CARTIVA, INC·Product code PNW·November 9, 2020
EVOLIS CEMENTED FIXED FEMUR SIZE 4 LEFT
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL, SA·Product code JWH·November 14, 2014
SPACELABS ULTRAVIEW SL COMMAND MODULE
FDA Adverse Event
Malfunction
·SPACELABS MEDICAL INC.·Product code DSI·April 26, 2013
INFINITI VISION SYSTEM OZIL
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·April 22, 2011
IPG NEURO
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·July 24, 2008
VERCISE CARTESIA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code NHL·September 9, 2021
Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone
FDA Enforcement
Class II
·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012