7 results
·
27ms
·
Sources: EU EUDAMED, US FDA
OHIO NON-REUSABLE TRACHEAL TUBE MURPHY
FDA 510(k)
FDA Class 2
·Anesthesiology
ERA® Implant Abutment Micro Ang. Base, 3mm Cuff (B)
FDA UDI
STERNGOLD DENTAL LLC·00841549105494·Implant retained overdentures are an establishe...
EXEL HUBER INFUSION SET WITH NEEDLELESS INJECTION SITE
FDA 510(k)
FDA Class 2
·General Hospital
REST ASSURED READY TO WEAR NITE PROTECTOR
FDA 510(k)
FDA Unclassified
·Unknown
MULTI-LINK 8
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code MAF·May 15, 2014
CAPSUREFIX
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012
ADVANTA BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·August 12, 2010