16 results · 38ms · Sources: EU EUDAMED, US FDA

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INSTANT-VIEW PROPOXYPHENE (PPX) URINE TEST

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

COATED VICRYL PLUS ANTIBACTERIAL SUTURE

FDA Adverse Event
Injury ·ETHICON, INC.·Product code GAM·April 20, 2006

COATED VICRYL PLUS ANTIBACTERIAL SUTURE

FDA Adverse Event
Injury ·ETHICON, INC.·Product code GAM·April 20, 2006

COATED VICRYL PLUS ANTIBACTERIAL SUTURE

FDA Adverse Event
Injury ·ETHICON, INC.·Product code GAM·April 20, 2006

COATED VICRYL PLUS ANTIBACTERIAL SUTURE

FDA Adverse Event
Injury ·ETHICON, INC.·Product code GAM·April 20, 2006

FLEXIBLE OCCLUSION SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

DINAMAP PRO 1000 MONITOR, MODEL 1000

FDA 510(k)
FDA Class 2 ·Cardiovascular

COATED VICRYL PLUS ANTIBACTERIAL SUTURE

FDA Adverse Event
Injury ·ETHICON, INC.·Product code GAM·April 25, 2006

COATED VICRYL PLUS ANTIBACTERIAL SUTURE

FDA Adverse Event
Injury ·ETHICON, INC.·Product code GAM·April 21, 2006

CAPIOX HEMOCONCENTRATOR

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code KDI·March 3, 2016

PEDFUSE PEDICLE SCREW DRIVER

FDA Adverse Event
Malfunction ·SPINEFRONTIER·Product code MNI·March 20, 2013

UNKNOWN DEPUY ASR ACETABULAR CUP

FDA Adverse Event
Malfunction ·DEPUY INTL LTD·Product code KWA·February 24, 2011

EMBRACE PUMP

FDA Adverse Event
Malfunction ·ROSS PRODUCTS DIVISION·Product code LZH·March 28, 2008

CAPIOX RX OXYGENATOR

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 31, 2024

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

The Propaq LT Series monitors. Model numbers 802LTAN, 802LT0N, and 802LTRN. These devices are indicated for ECG, noninvasive blood pressure (NIBP), respiration and SpO2. The most likely locations for patients to be monitored by these devices are hospital general medical-surgical, telemetry, and intermediate care floors, hospital emergency departments, transport, emergency medical services, and other healthcare applications. intended to be used by clinicians and medically qualified personnel for single or multiparameter vital signs monitoring of ambulatory and nonambulatory patients, including neonate, pediatric and adult patients. These devices are indicated for ECG, noninvasive blood pressure (NIBP), respiration and SpO2. The most likely locations for patients to be monitored by these devices are hospital general medicalsurgical, telemetry, and intermediate care floors, hospital emergency departments, transport, emergency medical services, and other healthcare applications. The monitors can be used as stand-alone devices or as devices networked to an Acuity Central Station through wireless communication over a Welch Allyn FlexNet network.

FDA Enforcement
Class II ·Terminated·Welch Allyn Protocol, Inc·January 15, 2014