19 results
·
22ms
·
Sources: EU EUDAMED, US FDA
PEEP VALVE
FDA 510(k)
FDA Class 2
·Anesthesiology
Couture Essence
FDA UDI
Carolon Company·00078301884049·
Couture Essence
FDA UDI
Carolon Company·00078301820443·
STRADIS
FDA UDI
STRADIS MEDICAL, LLC·M7528204040·STERILE SEPARATE-GAUZE 4X4
STRADIS
FDA UDI
STRADIS MEDICAL, LLC·M7528204041·STERILE SEPARATE-GAUZE 4X4
UniTip Catheter
FDA UDI
Unisensor AG·07640172971659·
UniTip Catheter
FDA UDI
Unisensor AG·07640172972274·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971642·
UniTip Catheter
FDA UDI
Unisensor AG·07640172972328·
UniTip Catheter
FDA UDI
Unisensor AG·07640172972311·
UniTip Catheter
FDA UDI
Unisensor AG·07640172972335·
MERZ DENTAL GMBH ARTEGRAL HD PREFORMED PLASTIC DENTURE TEETH
FDA 510(k)
FDA Class 2
·Dental
STERRAD NX with ALLClear Technology
FDA 510(k)
FDA Class 2
·General Hospital
ROSA RECON PLATFORM 220V
FDA Adverse Event
Injury
·ZIMMER CAS·Product code OLO·July 16, 2021
STYLE 68 SALINE FILLED BREAST IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FWM·October 3, 2017
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 9, 2014
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 31, 2012
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 5, 2015
Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.
FDA Enforcement
Class II
·Terminated·STERILMED, INC.·December 16, 2015