76 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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POWDER-FREE NITRILE EXAMINATION GLOVES, BLUE
FDA 510(k)
FDA Class 1
·General Hospital
EVONOS
FDA UDI
Gyrus ACMI, LLC·00821925012929·AUSTIN TYMPANOPLASTY HOOK
NA
FDA UDI
Nucletron B.V.·08717213043794·seedSelectron Treatment Accessories, Sterile (R...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450049556·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450188910·
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197044127·Potts-Smith Dressing Forceps
straig...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197044134·Waugh delicate dissecting forceps
200mm,...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197044141·Potts-Smith Dressing Forceps
straig...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197044158·Potts-Smith Dressing Forceps
straig...
PHILIPS MP60, MP70 AND MP90 INTELLIVUE PATIENT MONITORS WITH PORTAL TECHNOLOGY AND M3185 OPT C41 WIRELESS BEDSIDE ADAPTR
FDA 510(k)
FDA Class 2
·Cardiovascular
DISPOSABLE REFLECTIVE MARKER SPHERES
FDA 510(k)
FDA Class 2
·Neurology
SCHILLER
FDA UDI
SCHILLER MEDICAL·07613365900040·SpO2 Adult sensor for MAGLIFE Serenity
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 27, 2025
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 24, 2013
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·September 19, 2014
REMB OSC SAW
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code HBE·May 5, 2011
Allura Xper FD10C; Model Number: 722001; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
FDA Recall
Open, Classified
·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands·Product code OWB·September 3, 2025
Allura Xper CV20; Model Numbers: 722031; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
FDA Recall
Open, Classified
·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands·Product code OWB·September 3, 2025
Allura Xper FD20/20; Model Numbers: 722038; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
FDA Recall
Open, Classified
·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands·Product code OWB·September 3, 2025
Allura Xper FD20/15; Model Numbers: 722058; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
FDA Recall
Open, Classified
·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands·Product code OWB·September 3, 2025