11 results
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25ms
·
Sources: EU EUDAMED, US FDA
ROTACUBE
FDA 510(k)
FDA Class 1
·Microbiology
Snowden-Pencer
FDA UDI
STERIS CORPORATION·10885403152610·Snowden-Pencer DIAMOND-TIP OSTEOTOMES RISTOW 20...
dentaform®
FDA UDI
DENTAURUM GmbH & Co.KG·J011884017180·dentaform® Band, Tooth 46, Size 17/Roth 18
dentaform®
FDA UDI
DENTAURUM GmbH & Co.KG·J011884017000·dentaform® Band, Tooth 46, Size 17
dentaform®
FDA UDI
DENTAURUM GmbH & Co.KG·J011884017220·dentaform® Band, Tooth 46, Size 17/Roth 22
CHOCOLATE AGAR W/CHEMICALLY DEFINED
FDA 510(k)
FDA Class 1
·Microbiology
MICROTENS 7757 T.E.N.S. STIMULATOR
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
SMARTSITE EXTENSION SE
FDA Adverse Event
Malfunction
·CAREFUSION CORP·Product code FPA·February 12, 2014
PRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 14, 2010
IMHS CP NAIL
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JDS·December 21, 2012
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