10 results
·
24ms
·
Sources: EU EUDAMED, US FDA
SECHRIST DISPOSABLE INFANT BREATHING CIRCUIT
FDA 510(k)
FDA Class 1
·Anesthesiology
AQUA-PAD FOR MOIST OR DRY HEAT THERAPY
FDA 510(k)
FDA Class 2
·Physical Medicine
T4 CLASP-BEAD EIA KIT
FDA 510(k)
FDA Class 2
·Clinical Chemistry
INSPIRA TEXTURED SILICONE GEL FILLED BREAST IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FTR·October 15, 2024
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 26, 2014
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·January 3, 2013
ATLAS II HF CRT-D
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·November 10, 2010
SROM STM ST,36+6L NK,11X16X150
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code MRA·May 3, 2012
S-ROM*SLEEVE PRX ZTT, 16B-LRG
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code MRA·May 3, 2012
PINNACLE MTL INS NEUT36IDX54OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·March 23, 2012