11 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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F5
FDA 510(k)
FDA Class 2
·Physical Medicine
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526550193·GENUMEDI PT KNEE SUP SILVER R EW IV
LEONE SPA
FDA UDI
LEONE SPA·08033707011729·CALIBRA 1ST MOL BANDS W/G8025-03 n.UL 14
PRINCETON
FDA UDI
Princeton Medical Group, Inc.·00810158213098·UTERINE DILATOR HANK FIG. 13/14 DOUBLE ENDED 6....
MIRADRY SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
POWDER FREE NATURAL RUBBER LATEX PATIENT EXAMINATION GLOVES WITH LABELING PROTEIN CONTENT CLAIM (50 MICROGRAMS OR LESS)
FDA 510(k)
FDA Class 1
·General Hospital
POWERHEART G5 AUTOMATIC AED
FDA Adverse Event
Malfunction
·CARDIAC SCIENCE CORPORATION·Product code MKJ·October 18, 2018
ROTATING MULTIPLE CLIP APPLIER
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·June 3, 2013
530G INSULIN PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code OZO·September 27, 2014
ACRYSOF
FDA Adverse Event
Injury
·ALCON RESEARCH LTD. / HUNTINGTON·Product code HQL·June 23, 2011
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Injury
·ZOLL MANUFACTURING CORPORATION·Product code MVK·August 3, 2016