11 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CODMAN STERILIZATION CONTAINERS
FDA 510(k)
FDA Class 2
·General Hospital
ENDIUS ENDOSCOPIC ACCESS SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
DEVILBISS SLEEP RECORDER MODEL # RM60
FDA 510(k)
FDA Class 2
·Anesthesiology
POWERLINK SYSTEM
FDA Adverse Event
Injury
·ENDOLOGIX, INC.·Product code MIH·November 23, 2009
SOL-MILLENNIUM
FDA Adverse Event
Malfunction
·SOL-MILLENNIUM MEDICAL INC·Product code FMF·May 16, 2025
AUTOPLEX SYSTEM WITH VERTAPLEX HV W/O NEEDLES
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-PUERTO RICO·Product code JDZ·May 3, 2013
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·September 5, 2014
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 2, 2011
AS VEGA PS FEMORAL COMP.CEMENTED F7L
FDA Adverse Event
Injury
·AESCULAP AG·Product code JWH·February 25, 2020
AS VEGA PS FEMORAL COMP.CEMENTED F7L
FDA Adverse Event
Injury
·AESCULAP AG·Product code JWH·March 3, 2020
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