97 results
·
32ms
·
Sources: EU EUDAMED, US FDA
HEARLAB ACA
FDA 510(k)
FDA Class 2
·Neurology
NOVO Health Services, LLC
FDA UDI
NOVO HEALTH SERVICES, LLC·00812564032485·ANESTHESIA N/S EMESIS BASIN
Tasso Mini
FDA UDI
Tasso Inc.·00850038691141·
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K1230010·Rod Holder, Straight, 5.5 mm
N.A.
FDA UDI
DENTAURUM GmbH & Co.KG·J011123701000·Adhesive residue remover, wheel
ADVIA Centaur® Sample Cups
FDA UDI
Siemens Healthcare Diagnostics Inc.·00630414221571·
ADVIA CHEMISTRY LIQUID SPECIFIC PROTEIN CALIBRATORS
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ANGIONEW-IV
FDA 510(k)
FDA Class 2
·Cardiovascular
GMK-SPHERE REVISION FIXED TIBIAL TRAY CEMENTED SIZE 2 R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·August 21, 2019
BD NEXIVA¿ 24GA 0.75IN Y
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 21, 2018
BD NEXIVA¿ CLOSED IV CATHETER SYSTEM
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·October 30, 2018
KYPHON EXPRESS II INFLATABLE BONE TAMP
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code HRX·June 10, 2018
KYPHON EXPRESS¿ II INFLATABLE BONE TAMP
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO·Product code HRX·January 20, 2022
KYPHON® EXPRESS¿ II INFLATABLE BONE TAMP
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO S. DE R.L DE C.V.·Product code HRX·November 28, 2018
HUDSON VOLDYNE 2500 VOLUMETRIC EXCERCISER
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code BWF·May 14, 2013
SEE H-10
FDA Adverse Event
Injury
·STAAR SURGICAL COMPANY·Product code HQL·September 26, 2014
ADAPTA SR
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code NVZ·June 14, 2011
KYPHON EXPRESS II INFLATABLE BONE TAMP
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code HRX·June 29, 2018
KYPHON EXPRESS II INFLATABLE BONE TAMP
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code HRX·June 29, 2018
KYPHON® EXPRESS¿ INFLATABLE BONE TAMP
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code HRX·April 25, 2017