25 results · 25ms · Sources: EU EUDAMED, US FDA

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EARSCOPE

FDA 510(k)
FDA Class 1 ·Ear, Nose, Throat

SureStep™ Foley Tray System Bard® Lubricath Foley

FDA UDI
C. R. Bard, Inc.·00801741073960·SureStep® Foley Tray System Bard® Lubricath® Fo...

MGB Alert Internal Control Set MS2-E

FDA UDI
Elitechgroup Mdx LLC·03661540951442·The MGB Alert Internal Control Set MS2-E consis...

Bard® Urine Meter Foley Catheter Tray With Bard® Hydrophilic-Coated Foley

FDA UDI
C. R. Bard, Inc.·00801741020124·Bard® Urine Meter Foley Catheter Tray With Bard...

NAR Kit

FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209101528·KIT, RESCUE TASK FORCE VEST w' SIDE ARMOR - BLK

Elite Orthopaedics

FDA UDI
Elite Orthopaedics, Inc.·00816591013998·OA Knee Brace, Single Upright, Right

ACUMED

FDA UDI
Acumed LLC·10806378041570·Lkg RH Tray Insert Base

AcQMap®

FDA UDI
ACUTUS MEDICAL, INC.·00857042007210·Patient Electrode Kit 900100

Marina Medical

FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306810176·Hoyos 3-Hole Harvester, 9G x 30cm, 60cc

Elite Orthopaedics

FDA UDI
Elite Orthopaedics, Inc.·00816591014001·OA Knee Brace, Single Upright, Left

AcQMap

FDA UDI
ACUTUS MEDICAL, INC.·00857042007036·AcQMap® Patient Electrode Kit

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197491440·Titanium Blade 51x102...

Marina Medical

FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306835421·Pre-Assembled 3-Hole Hoyos Harvester, 09GA X 30...

MORCE POWER PLUS AND VARIOCARVE MORCELLATOR

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

ACCU-CHEK ADVANTAGE METER

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

BARD® LUBRICATH® FOLEY CATHETER

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZC·June 6, 2019

Catalog A800365, SureStep" Foley Tray, Bard LubricathTM Foley Catheter Tray

FDA Enforcement
Class II ·Ongoing·C.R. Bard Inc·September 29, 2021

UNKNOWN- UNSPECIFIED BY COMPLAINANT

FDA Adverse Event
Injury ·COOK BIOTECH, INC.·Product code FTM·April 3, 2014

ACCU-CHEK ® AVIVA PLUS TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 22, 2012

FREESTYLE FLASH

FDA Adverse Event
Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·September 28, 2007