12 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
TITANIUM ALLOY SONGER CABLE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668113189·STERILIZING CASE SMALL KATENA IOP
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668110942·STERILIZING CASE PLASTIC SMALL
Grasping forceps
FDA UDI
SOPRO-COMEG GmbH·04059082022611·
Washing Solution
FDA UDI
Phadia AB·07333066019505·Contains two bottles each of Washing Solution A...
PLAYTEX DEODORANT TAMPONS, MODEL 34902
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
GE VIVID E9 DIAGNOSTIC ULTRASOUND IMAGING SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
UNKNOWN PRODUCT - SET SCREW
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS KIEL·Product code HWC·October 12, 2012
670G INSULIN PUMP MMT-1780KL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·December 8, 2021
COLLEAGUE SINGLE CHANNEL VOLUMETRIC PUMP CE FRENCH
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·December 10, 2010
MINICAP TRANSFER SET
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·July 8, 2014
AUTOPULSE RESUSCITATION SYSTEM MODEL 100
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION, INC.·Product code DRM·December 17, 2012