10 results
·
28ms
·
Sources: EU EUDAMED, US FDA
DOUBLE SPRINGERS NONOXNOL 9 CONDOM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Natus
FDA UDI
XLTEK·00382830022248·NEUROWORKS 8.0.0 INTL DVD
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033449103·
INSET GUARD
FDA Adverse Event
Injury
·UNOMEDICAL A/S·Product code FPA·October 24, 2025
NEURO N100 RADIOFREQUENCY GENERATOR AND ACCESSORY CABLES
FDA 510(k)
FDA Class 2
·Neurology
XLTEK EVOKED POTENTIAL HEADBOX, MODEL EP-8
FDA 510(k)
FDA Class 2
·Neurology
TOTALCARE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·February 26, 2013
ACCU-CHEK SPIRIT
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·March 4, 2011
TAXUS EXPRESS2 PACLITAXEL - ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·Product code NIQ·March 13, 2008
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