10 results
·
21ms
·
Sources: EU EUDAMED, US FDA
J&S IRON REAGENTS
FDA 510(k)
FDA Class 1
·Clinical Chemistry
2.4MM SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036065300·2.7X16MM HIGH TORQUE CROSS-DRIVE SCREW
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450291948·
OSTEON II
FDA 510(k)
FDA Class 2
·Dental
MAINSTREAM WATER PURIFICATION DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
XLD 110V L.A. REF
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·May 14, 2014
ON-Q PAIN PUMP
FDA Adverse Event
Injury
·I-FLOW, LLC·Product code MEB·January 8, 2013
LIGAMAX-5MM ENDO CLIP APPLIER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·December 2, 2010
"2.4MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code HWC·April 15, 2019
"2.4MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code HWC·April 15, 2019