25 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ACE SDS 3.75MM SCREW DENTAL IMPLANT
FDA 510(k)
FDA Class 2
·Dental
artVeneer life
FDA UDI
Merz Dental GmbH·D7092002075·artVeneer life lower posteriors, M, B3
Silverbolt/Mainframe
FDA UDI
Choice Spine, LP·00840996170802·SILVERBOLT,SCREW,POLYAXIAL,5.5X75
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112601·BARRON CORNEAL PUNCH 7.25MM
AOS CAPTURED CORTICAL SCREW 4.2mm x 75.0mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665019520·
Golden Isles Pedicle Screw System
FDA UDI
Intelivation, LLC·G079C2520020750·Curved Cobalt Chrome Rod, Extended Hex
RIVA Posterior Fixation System
FDA UDI
XENIX MEDICAL LLC·00840493418346·CONSTRAINED STRAIGHT ROD, 6.0mm x 75mm
RIVA Posterior Fixation System
FDA UDI
XENIX MEDICAL LLC·00840493414102·Awl-Tip Iliac Tap, 7.5mm
RIVA Posterior Fixation System
FDA UDI
XENIX MEDICAL LLC·00840493418049·CONSTRAINED STRAIGHT ROD, 5.5mm x 75mm
DATEX-OHMEDA TEC 6 PLUS ANESTHESIA VAPORIZER, DATEX-OHMEDA TEC 6 PLUS NAD VARIANT ANESTHESIA
FDA 510(k)
FDA Class 2
·Anesthesiology
BOLUSPRO ULTRA
FDA 510(k)
FDA Class 2
·Radiology
NI
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code LHI·May 13, 2022
VENTED MICRO VOL.INLET, N/S
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code LHI·March 28, 2022
STORZ LED LIGHT SOURCE, EIN: 751-002075
FDA Adverse Event
Other
·KARL STORZ SE & CO. KG·Product code NTN·June 28, 2024
VALVE SET, EM2400
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code LHI·April 7, 2022
VALVE SET, EM2400
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code LHI·August 8, 2022
RESTORE ULTRA
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·March 13, 2013
TRANSTAR STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FPO·February 4, 2011
TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code NIQ·February 20, 2008
250 ML TPN BAG
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code LHI·May 21, 2021