19 results · 22ms · 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.

NIAGARA TEMPORARY DUAL LUMEN CATHETERS; FLEXXICON II TEMPORARY DUAL LUMEN CATHETERS

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

ELECTRODE LEADS 030-267 & 030-268

FDA 510(k)
FDA Class 3 ·Cardiovascular

HARDYDISK, AMPICILLIN, 10MCG

FDA 510(k)
FDA Class 2 ·Microbiology

Z-TOUCH

FDA 510(k)
FDA Class 2 ·Neurology

TRIAGE CARDIAC TRIPLE MARKER PANEL

FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 12, 2018

TRIAGE CARDIAC HS PANEL

FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 22, 2019

TRIAGE CARDIAC TRIPLE MARKER PANEL

FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR, INC.·Product code MMI·May 18, 2018

TRIAGE CARDIAC PANEL KIT

FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR, INC.·Product code JHX·April 18, 2018

TRIAGE CARDIAC HS PANEL

FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 21, 2019

TRIAGE CARDIAC TRIPLE MARKER PANEL

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code MMI·October 5, 2017

STYLE 410 COHESIVE SILICONE GEL FILLED BREAST IMPLANT

FDA Adverse Event
Injury ·ALLERGAN·Product code FTR·March 28, 2013

E SERIES DEFIBRILLATOR

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 21, 2011

MILLENNIUM MICROSURGICAL SYSTEM

FDA Adverse Event
Injury ·BAUSCH & LOMB·Product code HQC·April 17, 2008

TRIAGE CARDIAC TRIPLE MARKER PANEL

FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·November 1, 2018

BD INSULIN SYRINGE WITH BD ULTRA-FINE NEEDLE

FDA Adverse Event
Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·September 18, 2020

TRIAGE CARDIAC TRIPLE MARKER PANEL

FDA Adverse Event
Injury ·ALERE SAN DIEGO, INC.·Product code MMI·May 17, 2017

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

Aurora 4 Series, Aurora 7 lighthead; Models: AUA7 (including TV models). The Aurora Series is intended to illuminate the surgical field and ensure visibility of the surgical site.

FDA Enforcement
Class II ·Ongoing·DKK Dai-Ichi Shomei Co., Ltd.·August 21, 2024

The Spirit Select Bed, Model 5700 Spirit Plus /with high rail siderail option

FDA Enforcement
Class II ·Terminated·Stryker Medical Division of Stryker Corporation·November 21, 2018