13 results · 19ms · Sources: EU EUDAMED, US FDA

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XCEL 255 SLIT LAMP

FDA 510(k)
FDA Class 2 ·Ophthalmic

Needle Holder

FDA UDI
KATENA PRODUCTS, INC.·00841668108369·ANIS NEEDLE HOLDER STRAIGHT WITH LOCK

TI-DBLE LEAD CORT SCR

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code HSB·August 24, 2018

ADVIA 1650 CHOLINESTERASE ASSAY

FDA 510(k)
FDA Class 1 ·Clinical Toxicology

CANNON DIGITAL RADIOGRAPHY MODEL CXDI-40G

FDA 510(k)
FDA Class 2 ·Radiology

WALLFLEX DUODENAL

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code MUM·January 22, 2025

DIMENSION VISTA®

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code MMI·August 28, 2018

E SERIES DEFIBRILLATOR

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 3, 2013

LP ACCESSORY KIT, TRANSVERSE SINUS INTRODUCER PKG

FDA Adverse Event
Injury ·ST. JUDE MEDICAL·Product code OCL·April 14, 2011

COAGUCHEK S SYSTEM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·June 19, 2008

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

CADD¿- Solis Ambulatory Infusion Pump, Model 2111 & 2112, Version 1.0, Version 2.0 and Version 3.0 & Model 2120, Version 1.0. Provide measured drug therapy to patients in hospital or outpatient settings.

FDA Enforcement
Class II ·Terminated·Smiths Medical ASD, Inc.·June 24, 2015

Copeland HA Resurfacing Head, MB/HA EAS Head; Item Nos. 11-114641 11-114642 11-114643 11-114644 11-114644S 11-114645 11-114646 11-114647 11-114648 11-114661 11-114662 11-114663 11-114664 11-114664S 11-114665 11-114666 11-114667 11-114668 11-114632 11-114633 Product Usage: Partial Shoulder Replacement.

FDA Enforcement
Class II ·Terminated·Zimmer Biomet, Inc.·December 4, 2019