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

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PERIOPHIL BIPHASIC

FDA 510(k)
FDA Class 2 ·Dental

KSEA NEURO-FIBERSCOPE

FDA 510(k)
FDA Class 2 ·Neurology

VAPORIZED HYDROGEN PEROXIDE (VHP) STERILIZATION OF UNMWPE COMPONENTS IN THE COFIELD TOTAL SHOULDER SYSTEM, THE NEER II

FDA 510(k)
FDA Class 2 ·Orthopedic

BD INSULIN SYRINGE WITH BD ULTRA-FINE NEEDLE

FDA Adverse Event
Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·November 12, 2019

PORTABLE AIR COMPRESSOR FOR MEDICAL PURPOSES

FDA Adverse Event
Malfunction ·INVACARE SUZHOU·Product code BTI·May 3, 2013

TRILOGY 100

FDA Adverse Event
Malfunction ·RESPIRONICS, INC·Product code CBK·August 20, 2014

INTEGRITY RX CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code MAF·May 10, 2011

CAP FOR INJECTOR MEMBRANE M50

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·May 4, 2021

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