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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MODEL 295 ELECTRONIC RESPIROMETER
FDA 510(k)
FDA Class 2
·Anesthesiology
Brigade
FDA UDI
Nuvasive, Inc.·00887517964854·Brigade Lateral Trial, 17x38x32mm 12°
NEZHAT-DORSEY REUSABLE ELECTROSURGICAL ATTACHMENTS: J-HOOK TIP, L-HOOK TIP, CORBITT SPATULA TIP, NEEDLE TIP, BALL TIP
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
B Dispensing Line
FDA 510(k)
FDA Class 2
·General Hospital
SPACELABS
FDA Adverse Event
Injury
·SPACELABS HEALTHCARE·Product code MHX·May 16, 2013
QUADRA ASSURA CRT-D, DF-4 CONNECTOR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·June 30, 2014
INSTINCT JAVA SYSTEM GENERIC IMPLANT
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·January 4, 2013
ACCU-CHEK ® COMPACT TEST DRUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·November 20, 2010
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