9 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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A-DEC PAC I PORTABLE UNIT
FDA 510(k)
FDA Class 1
·Dental
BBIG
FDA UDI
BBig B.V.·08719616011660·4903451
Brigade
FDA UDI
Nuvasive, Inc.·00887517962638·Brigade Lateral Trial, 12x34x32mm 12°
DENVER PAK W/ DOUBLE-VALVE ASCITES SHUNT,DENVER PAK W/ SINGLE-VALVED ASCITES SHUNT, DENVER PAK, DOUBLED-VALVED ASCITES T
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
OMNIGUIDE BEAMPATH CO2 MARK III WAVEGUIDE FIBER WITH LOW PROFILE/LOW LOSS TIP
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ASR ACETABULAR CUPS 50
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD.-8010379·Product code KWA·June 30, 2014
NI
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code NKB·November 15, 2010
X-ACT ROM KNEE
FDA Adverse Event
Injury
·DJO, LLC·Product code IQI·January 4, 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