65 results
·
28ms
·
Sources: EU EUDAMED, US FDA
MODIFICATION TO T-REX BIOPSY FORCEPS
FDA 510(k)
FDA Class 2
·Cardiovascular
PowerPICC SOLO
FDA UDI
Bard Access Systems, Inc.·00801741096280·Catheter Placement Kit
TruFlex
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730014740·NiTi RCS Lower 20x20 10 archwires per pack
NiTi Archwires
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730013774·NiTi RCS Type 5 Lower 20x20 10 archwires per pack
TEWA
FDA UDI
asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282501754·TeWa 5CB-Type 3050 Speed Pak: coated acupunctu...
TEWA
FDA UDI
asia-med GmbH·04251282509071·TeWa 5CB-Type 3050 Speed Pak: coated acupunctu...
4WEB Medical
FDA UDI
4web Medical·00812998048779·
LIFEPAK® 12 defibrillator/monitor
FDA UDI
PHYSIO-CONTROL, INC.·00721902148835·LP12AABBAAAABAABAAAAAAAALP12 MONITOR-DEFIB
Admiral
FDA UDI
Seaspine Orthopedics Corporation·10889981239404·Trial Drill Guide, 9mm
SUNI MAX
FDA 510(k)
FDA Class 1
·Dental
SPIRAL RADIUS RODDING SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·September 2, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·September 2, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·September 2, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·September 2, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·September 2, 2021
N/A
FDA UDI
Zimmer, Inc.·00889024023123·
NA
FDA UDI
Zimmer, Inc.·00889024022973·
NA
FDA UDI
Zimmer, Inc.·00889024023031·
NA
FDA UDI
Zimmer, Inc.·00889024022911·