26 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HEMOGLOBIN A1C REAGENT SET
FDA 510(k)
FDA Class 2
·Hematology
External thermoplastic nasal splint
FDA UDI
Spiggle & Theis Medizintechnik GmbH·04250381810101·64x40x36 mm, standard, 1.6 mm
self-a...
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702250084·Elvarex 2/Thigh High/Slant-Open Toe-Elephantias...
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702261547·Elvarex Forte 3/Thigh High/Slant, Closed Toe, E...
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04059993024650·ELVAREX 2/BODY BAND WITHOUT LEG EXTENSION/BOTH...
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0112000·Inserter, Universal Inline Fixed
Mariner Outrigger
FDA UDI
Seaspine Orthopedics Corporation·10889981173234·L Con, Side-Loading, L, 8mm, 200mm
COMPAS
FDA 510(k)
FDA Class 2
·Anesthesiology
GILB, MODEL 8010
FDA 510(k)
FDA Class 2
·Dental
BD PHOENIX¿ SMIC-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 13, 2026
COMPRESSURE FRACTURE REPAIR IMPLANT
FDA Adverse Event
Injury
·USI ORTHOPAEDICS LLC DBA U.S. ORTHOPAEDICS·Product code HTN·April 6, 2011
CONSULTA CRT-D
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·April 10, 2013
COOK CELECT VENA CAVA FILTER
FDA Adverse Event
Malfunction
·WILLIAM COOK EUROPE APS·Product code DTK·May 22, 2008
AIRCAST CRYO/CUFF
FDA Adverse Event
Injury
·DJ ORTHOPEDICS DE MEXICO·Product code ILO·April 6, 2011
BD PHOENIX¿ SMIC/ID-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·October 16, 2024
BD PHOENIX¿ SMIC/ID-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 1, 2024
BD PHOENIX¿ SMIC-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 28, 2025
BD PHOENIX¿ SMIC-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 28, 2025
BD PHOENIX¿ SMIC-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 28, 2025
BD PHOENIX¿ SMIC/ID-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 8, 2024