10 results · 28ms · Sources: EU EUDAMED, US FDA

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TIDAL WAVE SP MODEL 710/715 AND 715

FDA 510(k)
FDA Class 2 ·Cardiovascular

Baltic Denture System BD Load

FDA UDI
Merz Dental GmbH·D7091032971·Baltic Denture System BDLoad ↓ Mn7 PLSEum2DFm C...

MTG - MINITUB HEATED STAGE SYSTEMS

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

ISOLA SPINAL SYSTEMS

FDA 510(k)
FDA Class 2 ·Orthopedic

EDWARDS SAPIEN TRANSCATHETER HEART VALVE

FDA Adverse Event
Malfunction ·EDWARDS LIFESCIENCES·Product code NPT·April 3, 2013

INSYNC MAXIMO

FDA Adverse Event
Death ·MEDTRONIC MED REL, INC.·Product code NIK·March 29, 2011

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 25, 2014

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

Smiths Medical Medfusion Model 4000 Syringe pump, Item Numbers: a) 4000-0101-249, b) 4000-0101-50, c) 4000-0101-51, d) 4000-0105-249, e) 4000-0105-50, f) 4000-0105-51, g) 4000-0105-78, h) 4000-0106-00, i) 4000-0106-01, j) 4000-0106-231,

FDA Enforcement
Class II ·Ongoing·Smiths Medical ASD Inc.·April 24, 2024

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