29 results · 20ms · Sources: EU EUDAMED, US FDA

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DRIED GRAM-POSITIVE MIC/COMBO PANELS

FDA 510(k)
FDA Class 2 ·Microbiology

BD PHOENIX¿ SMIC-101

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 13, 2026

BD PHOENIX¿ SMIC/ID-101

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·October 16, 2024

LOCATOR R-Tx

FDA UDI
Zest Anchors, LLC·00840481112881·LOCATOR R-Tx Abutment for Wide Platform (WP) Ex...

LOCATOR F-Tx

FDA UDI
Zest Anchors, LLC·00840481121166·LOCATOR F-Tx Abutment for Wide Platform (WP) Ex...

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

BD PHOENIX¿ SMIC/ID-101

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·December 12, 2024

BD PHOENIX¿ SMIC/ID-101

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 19, 2026

BD PHOENIX¿ SMIC/ID-101

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 19, 2026

BD PHOENIX¿ SMIC/ID-101

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 19, 2026

BD PHOENIX¿ SMIC/ID-101

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 19, 2026

CosmoLock Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07311K0112020·Tap, 4.75 mm

NIDO Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07315K0112020·Tap, 4.75mm

ULTRAQUIET

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

MSI BIPOLAR SHEATH

FDA 510(k)
FDA Class 2 ·Orthopedic

M-LNCS DC-I

FDA Adverse Event
Malfunction ·MASIMO - 40 PARKER·Product code DQA·November 21, 2016