23 results · 23ms · Sources: EU EUDAMED, US FDA

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NIPRO SAFETOUCH PSV SCALP VEIN SET WITH SAFETY DEVICE

FDA 510(k)
FDA Class 2 ·General Hospital

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·00636257125168·20-30 MV FOR MEN CLSC CALF STD TAN VI

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·00636257127292·20-30 MV FOR MEN SEL CALF STD TAN VI

Fuji Cervical Plate System

FDA UDI
Altus Spine, LLC·B41711401361·36mm Level 1 Cervical Plate System - Fuji

Hayden Medical

FDA UDI
Hayden Medical, Inc.·00840319720639·Rochester (Pean) Hemostatic Forceps 5-1/2" (14c...

RESPICHAMBER VALVED HOLDING CHAMBER

FDA 510(k)
FDA Class 2 ·Anesthesiology

EMBRYOGEN

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

Widex

FDA UDI
Widex A/S·05706069923544·WIDEX MOMENT MBB3D 440 (Deep blue)

Widex

FDA UDI
Widex A/S·05706069972344·WIDEX MOMENT MBB2 440 (Deep blue)

Widex

FDA UDI
Widex A/S·05706069715705·Widex EVOKE E-FA (Deep Blue ) 440, Telecoil, Vo...

Widex

FDA UDI
Widex A/S·05706069718317·Widex EVOKE E-FM (Deep Blue ) 440, RC coil

Widex

FDA UDI
Widex A/S·05706069716054·Widex EVOKE E-FP (Deep Blue ) 440, Telecoil, Vo...

Widex

FDA UDI
Widex A/S·05706069884630·WIDEX MOMENT MRR2D (Deep Blue ) 440, RC coil, m...

ULTRAMINI

FDA Adverse Event
Injury ·LIFESCAN, INC.·Product code NBW·September 18, 2007

ENDO GIA ADAPTER XL

FDA Adverse Event
Malfunction ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GAG·October 3, 2014

VASO VIEW HEMOPRO

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·May 29, 2013

COLLEAGUE PRE-P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 25, 2011

ARCHITECT C16000 SYSTEM

FDA Adverse Event
Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·June 26, 2019

ONE TOUCH ULTRAMINI METER

FDA Adverse Event
Injury ·LIFESCAN, INC.·Product code NBW·February 22, 2010

AQUAPAK 640 SW, 650ML W/040 ADAPTOR, INTL. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor packaged with the water bottle is affected by this recall.

FDA Enforcement
Class II ·Terminated·Teleflex Medical·February 18, 2015