15 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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COCOON CONVECTIVE WARMING SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
Gyrus ACMI
FDA UDI
Gyrus ACMI, LLC·00821925015975·SHEA PLAT-FLPL CP PIST
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613017743·K-Wire, Double Ended, Trocar Point, Diameter Si...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197056649·Kelly Hemostatic Forceps Fig. 2
190mm,...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197056663·Kelly Hemostatic Forceps Fig. 2
240mm,...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197056656·Kelly Hemostatic Forceps Fig. 2
220mm,...
REMINGTON I-LIGHT HAIR REMOVAL SYSTEM
FDA Adverse Event
Injury
·SHASER INC·Product code ONF·May 21, 2021
SPECTRA WAVEWRITER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 16, 2023
CARRARA INTERACTION CERAMIC SYSTEM
FDA 510(k)
FDA Class 2
·Dental
ARROWGARD EVOLUTION ANTIMICROBIAL PERIPHERALLY INSERTED CENTRAL CATHETER (PICC) MODEL: S-44041-002, S-45041-002, S-45504
FDA 510(k)
FDA Class 2
·General Hospital
23 X 0.75 IN. NEEDLE X 12 IN TUBING BD SAFETY-LOK¿ BLOOD COLLECTION WINGSET
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·December 14, 2016
23 X 0.75 IN. NEEDLE X 12 IN TUBING BD SAFETY-LOK¿ BLOOD COLLECTION WINGSET
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·December 14, 2016
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·May 31, 2013
PAD CONNECTOR CABLE
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code MKJ·June 16, 2011
LEVEEN NEEDLE ELECTRODE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code GEI·August 28, 2008