17 results
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26ms
·
Sources: EU EUDAMED, US FDA
HEMAT 12
FDA 510(k)
FDA Class 2
·Hematology
RAD
FDA UDI
MEDTRONIC XOMED, INC.·20763000518138·BLADE 1884006 RAD40 5PK SINUS 4MM
RAD®
FDA UDI
MEDTRONIC XOMED, INC.·20681490047474·BLADE 1884006 RAD40 5PK SINUS 4MM
Cross-Linked PE Insert
FDA UDI
ADLER ORTHO SPA·08050507130269·Cross-Linked PE Insert 15° Lipped Diam. 28 Gr. C
Reprocessed 4.0mm Rad 40 Curved Blade
FDA UDI
SURETEK MEDICAL·B39018840061·Reprocessed 4mm Rad 40 Curved Blade
Ormco
FDA UDI
ORMCO CORPORATION·00889989013979·5DEG SHEATH-R 036 W/BHK EA
dentaform®
FDA UDI
DENTAURUM GmbH & Co.KG·J011884006180·dentaform® Band, Tooth 46, Size 6/Roth 18
dentaform®
FDA UDI
DENTAURUM GmbH & Co.KG·J011884006000·dentaform® Band, Tooth 46, Size 6
dentaform®
FDA UDI
DENTAURUM GmbH & Co.KG·J011884006220·dentaform® Band, Tooth 46, Size 6/Roth 22
BRUCELLA MEDIA
FDA 510(k)
FDA Class 1
·Microbiology
PLASTELAST AND/OR ELASTOPLASTE
FDA 510(k)
FDA Class 1
·General Hospital
VOYAGER NC CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code LOX·December 21, 2012
TRANSTAR STRETCHER
FDA Adverse Event
Malfunction
·HILLROM DE MEXICO S DE RL DE CV·Product code FPO·February 14, 2014
BIPAP DEVICE
FDA Adverse Event
Death
·RESPIRONICS INC.·Product code BZD·October 14, 2010
XPS® BLADE
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code EQJ·November 17, 2017
XPS® BLADE
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code EQJ·March 5, 2025
DATEX-OHMEDA S/5 SINGLE-WIDTH AIRWAY MODULE, E-MINIC AND ACCESSORIES. DATEX-OHMEDA S/5TM FM WITH L-FICU04 ANDL-FICUO4A SOFTWARE AND N-FCREC MODULE **(OUS only). E-miniC and accessories is indicated for monitoring C02 and respiration rate of all hospital patients.
FDA Enforcement
Class I
·Terminated·GE Healthcare, LLC·July 30, 2014