9 results
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19ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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KEJUMP DIGITAL CLINICAL THERMOMETER
FDA 510(k)
FDA Class 2
·General Hospital
Brigade
FDA UDI
Nuvasive, Inc.·00887517964014·Brigade Lateral Trial, 7x38x32mm 20°
GRAMS POLYESTER NONABSORBABLE SUTURE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PLANMECA PROMAX 3D MAX
FDA 510(k)
FDA Class 2
·Dental
STEALTHSTATION¿ S8 SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·March 20, 2025
ULTRACISION * SURG DEV, BLADES 5MM, ENDO
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 30, 2014
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·November 16, 2010
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·January 9, 2013
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