8 results
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18ms
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Sources: EU EUDAMED, US FDA
K-LOK CATHETER SECUREMENT DEVICE MODIFICATION
FDA 510(k)
FDA Class 1
·General Hospital
SIC invent Dental Implant Systems
FDA UDI
SIC invent AG·04260516871143·SIC Depth Stop for Drill up to Ø 4.60 mm for L ...
Barco
FDA UDI
FIMI SRL·05415334002296·MDSC-8427 LED
PHILIPS P74P BEHIND-THE-EAR HEARING AID
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
ALOKA 680 DIAGNOSTIC ULTRASOUND SCANNING SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
8800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 14, 2013
SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER CORP, MEDICAL DIV.·Product code FNL·December 4, 2010
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE·Product code IOR·July 15, 2014