7,732 results · 44ms · Sources: EU EUDAMED, US FDA

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HO-B-LITE VI UNIT

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

HNM Women Care

FDA UDI
HNM STAINLESS, LLC.·00812171027577·DISPOSABLE LOOP ELECTRODES, 15mm x 7mm, STERILE...

HNM Women Care

FDA UDI
HNM STAINLESS, LLC.·00842962103364·DISPOSABLE LOOP ELECTRODES, 10mm x 7mm, STERILE...

HNM MEDICAL

FDA UDI
HNM STAINLESS, LLC.·00842962162422·DISPOSABLE LOOP ELECTRODES, 15mm x 7mm, STERILE...

GPS STRETCHER

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FPO·June 9, 2020

TOTALCARE SPO2RT

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code IOQ·November 14, 2016

HNM MEDICAL

FDA UDI
HNM STAINLESS, LLC.·00842962162392·DISPOSABLE LOOP ELECTRODES, 10mm x 7mm, STERILE

HNM Women Care

FDA UDI
HNM STAINLESS, LLC.·00842962100240·DISPOSABLE LOOP ELECTRODES, 10mm x 7mm, STERILE

HNM MEDICAL

FDA UDI
HNM STAINLESS, LLC.·00842962162439·DISPOSABLE LOOP ELECTRODES, 15mm x 7mm, STERILE

HNM Women Care

FDA UDI
HNM STAINLESS, LLC.·00842962100271·DISPOSABLE LOOP ELECTRODES, 15mm x 7mm, STERILE

STRYKER BED MODEL 1115 PRIME SERIES BIG WHEEL

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FNL·March 1, 2017

S3 MED/SURG BED

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FNL·June 13, 2016

TOTALCARE

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code IOQ·July 27, 2016

INTRACRANIAL PRESSURE MONITORING KIT

FDA Adverse Event
Malfunction ·INTEGRA NEUROSCIENCES·Product code GWM·December 19, 2007

SPORT TOTAL CARE

FDA Adverse Event
HILL-ROM·Product code FNL·October 20, 2010

IAB: 8FR-30 CC FOS

FDA Adverse Event
Malfunction ·ARROW INTL., INC.·Product code DSP·April 18, 2008

STERIS

FDA Adverse Event
Malfunction ·STERIS CORPORATION·Product code FQO·March 2, 2021

RHINO-LARYNGO VIDEOSCOPE

FDA Adverse Event
Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code EOB·September 23, 2022

ARJO CITADEL BED ARJO, ALTERNATING AIR BED,

FDA Adverse Event
Injury ·ARJOHUNTLEIGH POLSKA SP. ZO.O.·Product code FNL·March 8, 2021

EDOCS 120B-22

FDA Adverse Event
Malfunction ·PACIFIC CONSOLIDATED INDUSTRIES·Product code CAW·February 18, 2012