9 results · 20ms · Sources: EU EUDAMED, US FDA

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BIPAP AVAPS VENTILATORY SUPPORT SYSTEM

FDA 510(k)
FDA Class 2 ·Anesthesiology

NIRTRILE PATIENT EXAMINATION GLOVE (BLUE COLOR) POWDERED, NON STERILE

FDA 510(k)
FDA Class 1 ·General Hospital

HELICAL COMPRESSION ANCHOR SYSTEM, CANNULATED SINGLE HELIX

FDA 510(k)
FDA Class 2 ·Orthopedic

RAD-8

FDA Adverse Event
Malfunction ·MASIMO CORPORATION·Product code DQA·July 15, 2015

BD VACUTAINER® K3E 5.4MG PLUS BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·August 2, 2019

UNKNOWN ZIMMER KNEE

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JWH·May 11, 2011

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Injury ·BAXTER HEALTHCARE·Product code KDJ·May 3, 2013

SERVO-I

FDA Adverse Event
Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·August 20, 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