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

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Tempus Pro Patient Monitor

FDA 510(k)
FDA Class 2 ·Cardiovascular

DJO SURGICAL

FDA UDI
Encore Medical, L.P.·00190446857716·SPECIAL, EXPRT REVISION HIP DISTAL STEM TRIAL, ...

MSI

FDA UDI
Modern Surgical Instruments LLC·B4192017460·

HHM

FDA UDI
Oticon A/S·05707131351487·G500 SC, BTE PP 13 2.4G 105 C090 TAR HHM

MSI

FDA UDI
Modern Surgical Instruments LLC·00810130202034·6" Vein Retractor, with Loop Handle

CODMAN

FDA UDI
Cerenovus, Inc.·10886704001980·CODMAN SLIM-LINE Aneurysm Clip Reinforcing Angl...

7450 RV2 MASK

FDA UDI
HANS RUDOLPH, INC.·00817136022505·7450S FACE MSK-HEADGEAR-CC1808

Millennium

FDA UDI
Avalign Technologies, Inc.·00190776191863·VEIN RETRACTOR BLADE LENGTH WIDE

Symmetry Surgical

FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482057704·Symmetry® Retractor, Custom Vein, 6 in

SQA V, SPERM QUALITY ANALYZER

FDA 510(k)
FDA Class 2 ·Hematology

LIGHTSHEER PULSED DIODE ARRAY LASER SYSTEM (FAMILY OF PRODUCTS)

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

MERSILENE TAPE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code KDC·November 9, 2018

UNKNOWN COOL TIP ELECRTRODE

FDA Adverse Event
Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·March 3, 2020

GE OEC 6800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·October 21, 2008

HS III PROXIMAL SEAL SYSTEM 4.3MM

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·August 4, 2011

840 VENTILATOR

FDA Adverse Event
Injury ·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·June 28, 2013

ANIMAS INSULIN CARTRIDGE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·September 20, 2012

SYNERGY

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·September 25, 2015

UNK - CONSTRUCTS: PHILOS PLATE/SCREWS

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code HRS·June 10, 2021

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·April 9, 2019