9 results · 29ms · Sources: EU EUDAMED, US FDA

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CARBON FIBER COMPOSITE CIRCULAR FIXATION (CIRFIX) DEVICE (HALF RING)

FDA 510(k)
FDA Class 2 ·Orthopedic

Baltic Denture System BD Load

FDA UDI
Merz Dental GmbH·D7091032169·Baltic Denture System BDLoad ↓ Mn7 PLSEum2DFm A...

ILT SUPPORT CATHETER .014, MODEL C114LW1; ILT SUPPORT CATHETER ADVANCING MECHANISM, MODEL A11AM1

FDA 510(k)
FDA Class 2 ·Cardiovascular

GLIADIN IGA ANTIBODY EIA DETECTION SYSTEM

FDA 510(k)
FDA Class 2 ·Immunology

UNK LIGASURE INSTRUMENT

FDA Adverse Event
Malfunction ·COVIDIEN LP·Product code GEI·March 7, 2013

SYNCHRON® URIC ACID REAGENT

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code KNK·March 28, 2011

TERUMO ADVANCED PERFUSION SYSTEM 1

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code KRL·April 21, 2008

PANEL PHOENIX NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·December 21, 2023

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