9 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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DOLPHIN MEDICAL 2150 HANDHELD PULSE OXIMETER
FDA 510(k)
FDA Class 2
·Cardiovascular
BUSCH®, BNA®
FDA UDI
BUSCH & CO. GmbH & Co. KG·D8120306291·Diamond, medium grit
FLEXTIME
FDA 510(k)
FDA Class 2
·Dental
MTP RESESURFACING JOINT-SMALL/9301-01; MEDIUM/9301-02; LARGE/9301-03
FDA 510(k)
FDA Class 2
·Orthopedic
ULTRAPRO HERNIA SYSTEM
FDA Adverse Event
Injury
·ETHICON, INC.·Product code FTL·April 2, 2013
CENTRA BED
FDA Adverse Event
Malfunction
·HILL-ROM INC.·Product code FNL·March 22, 2011
COBAS 6000 C501 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CEM·April 15, 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
Boston Scientific COGNIS CRT-D, Cardiac Resynchronization Therapy Defibrillator, models N118, N119. The following models are not available in the US: models N106, N107, P106, P107. Sterilized using ethylene oxide. Boston Scientific, 4100 Hamline Avenue North, St. Paul, MN 55112-5798 USA. Indicated for patients who are at risk for sudden cardiac death due to ventricular arrhythmias and may require pacing support.
FDA Enforcement
Class II
·Terminated·Boston Scientific CRM Corp·October 23, 2013