16 results · 21ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

EVGUIDE TIP LOCATION SYSTEM

FDA 510(k)
FDA Class 2 ·General Hospital

PORTABLE BREAST COMPRESSION DEVICE

FDA 510(k)
FDA Class 1 ·Radiology

TWINFIX INTERFRAGMENTARY COMPRESSION SCREW SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

CAIMAN DISP. INSTR. NON ARTICUL. D:5/360MM

FDA Adverse Event
Malfunction ·AESCULAP AP & CO. KG·Product code GEI·March 27, 2015

CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM

FDA Adverse Event
Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

PRISMAFLEX

FDA Adverse Event
Injury ·GAMBRO LUNDIA AB·Product code KDI·May 6, 2010

PRISMAFLEX

FDA Adverse Event
Injury ·GAMBRO LUNDIA AB·Product code KDI·November 5, 2010

CAIMAN DISP.INSR.ARTICULAT.D:12 / 240MM

FDA Adverse Event
Malfunction ·AESCULAP AG& CO. KG·Product code GEI·April 15, 2015

CAIMAN DISP INSTR ARTICULAT D:12/240MM

FDA Adverse Event
Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 16, 2014

PRISMAFLEX

FDA Adverse Event
Injury ·GAMBRO LUNDIA AB·Product code KDI·November 25, 2010

GREENLIGHT MOXY FIBER OPTIC

FDA Adverse Event
Injury ·AMERICAN MEDICAL SYSTEMS·Product code GEX·April 30, 2013

POWERED WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE TAYLOR STREET·Product code ITI·September 16, 2014

ACCU-CHEK ® AVIVA TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 18, 2011

BD VACUTAINER® K2E 5.4MG PLUS BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·June 1, 2018

CAIMAN DISP. INSTR. ARTICULAT. D.: 12/440MM

FDA Adverse Event
Malfunction ·AESCULAP AG & CO. KG·Product code GEI·July 28, 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