8 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MODIFIED SURGIPORT DISPOSABLE TROCAR AND SLEEVE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Brigade
FDA UDI
Nuvasive, Inc.·00887517962317·Brigade Lateral Trial, 7x34x28mm 30°
RCRP FLEX REAGENT CARTRIDGE
FDA 510(k)
FDA Class 2
·Immunology
IVAS 2-10MM (10 GAUGE) BALLOON CATHETER, IVAS 2-15 MM(10 GAUGE)0705-115-500, IVAS 3-10MM(8 GAUGE)BALLOON CATHETER, IVAS
FDA 510(k)
FDA Class 2
·Orthopedic
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·June 30, 2014
NI
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code KWP·November 15, 2010
DRILL 3334800 VISAO 80K HANDPIECE
FDA Adverse Event
Malfunction
·MEDTRONIC INC.·Product code ERL·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