35 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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VULCAN ELECTROSURGICAL PROBES: VULCAN MICRO LIGAMENT CHISELS, VULCAN LIGAMENT CHISELS, VULCAN EFLEX LIGAMENT CHISELS
FDA 510(k)
FDA Class 2
·Orthopedic
Nobel
FDA UDI
Preat Corporation·00842092101377·NobelBiocare™ Tri-Lobe-compatible WP Snappy Abu...
PowerPICC Provena
FDA UDI
Bard Access Systems, Inc.·00801741136597·Catheter Placement Kit
AtriClip™ LAA Exclusion System
FDA UDI
ATRICURE, INC.·10840143906183·AtriClip® Gilinov-Cosgrove LAA Exclusion System 50
S NEEDLE
FDA UDI
asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282505448·asia-med s-needle J-Type 3050 Place N' Press: c...
AtriClip® Gillinov-Cosgrove® LAA Exclusion System
FDA UDI
ATRICURE, INC.·10840143911934·LAA Exclusion System, ACH150
AtriClip™ LAA Exclusion System
FDA UDI
ATRICURE, INC.·10840143900082·AtriClip® Gilinov-Cosgrove LAA Exclusion System 50
S NEEDLE
FDA UDI
asia-med GmbH·04251282512439·asia-med s-needle J-Type 3050 Place N' Press: c...
AtriClip™ LAA Exclusion System
FDA UDI
ATRICURE, INC.·00818354011449·AtriClip® Gilinov-Cosgrove LAA Exclusion System 50
AtriClip® Gillinov-Cosgrove™ LAA Exclusion System
FDA UDI
ATRICURE, INC.·10840143913358·LAA Exclusion System, ACH150
FlowLogic Assert
FDA UDI
SONENDO, INC.·00810209420956·FlowLogic Assert Shaping File .04 Kit, 25mm
MFCD 118
FDA 510(k)
FDA Class 2
·Radiology
DURACON SYMMETRIC METAL-BACKED PATELLAR COMPONENT
FDA 510(k)
FDA Class 2
·Orthopedic
PLATE BD CHROMAGAR O-157 20 EA
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code JSI·August 10, 2021
PLATE BD CHROMAGAR O-157 20 EA
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code JSI·August 10, 2021
OPTETRAK
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·August 6, 2019
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·March 12, 2013
VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBC IGM REAGENT
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code LOM·February 24, 2011
COBAS INTEGRA 800
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·February 15, 2008
OMNIPOD INSULIN MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code LZG·November 15, 2019