170 results
·
20ms
·
Sources: EU EUDAMED, US FDA
SUPER NOVA, ACUBEAM
FDA 510(k)
FDA Class 2
·Physical Medicine
SHIELDED SYRINGE CARRIER
FDA UDI
BIODEX MEDICAL SYSTEMS, INC.·00718175000762·Syringe Carrier, Large, .125" Lead
Syringe Carrier, Large 0.125" lead
FDA UDI
Mirion Technologies (capintec), Inc.·00859942006669·Leaded Syringe Carrier
artVeneer life
FDA UDI
Merz Dental GmbH·D7092001179·artVeneer life upper anteriors, IL, B1
UniTip Catheter
FDA UDI
Unisensor AG·07640172972007·
NUZONE NITRILE SURGICAL GLOVES POWDER FREE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
RECUMBENT BATHING SYSTEMS, RHAPSODY AND PRIMO
FDA 510(k)
FDA Class 2
·Physical Medicine
CARDIOSAVE HYBRID, TYPE B PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·August 29, 2024
CARDIOSAVE HYBRID, TYPE B PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·January 25, 2023
CARDIOSAVE HYBRID W/ E/F PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·January 30, 2023
INDIGO SYSTEM ASPIRATION CATHETER 8
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DXE·June 13, 2018
IMPAX CV REPORTING
FDA Adverse Event
Malfunction
·AGFA HEALTHCARE CORP.·Product code LLZ·February 26, 2013
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·February 24, 2011
ASCENSIA BREEZE2
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE, LLC·Product code NBW·February 15, 2008
CARDIOSAVE HYBRID, TYPE B PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·January 31, 2023
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·December 1, 2010
CARDIOSAVE HYBRID, TYPE B PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·October 5, 2023
NA
FDA UDI
Zimmer, Inc.·00889024034808·
NA
FDA UDI
Zimmer, Inc.·00889024034983·
NA
FDA UDI
Zimmer, Inc.·00889024034624·