33 results · 28ms · Sources: EU EUDAMED, US FDA

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MICRUS STRETCH-RESISTANT MICROCOIL SYSTEM, MSR01

FDA 510(k)
FDA Class 2 ·Neurology

CD HORIZON® Spinal System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994325563·CONNECTOR 7022420 LAT CONN SS 6.35 22MM

GALILEO® TROCHANTERIC NAIL, LEFT, Ø11mm x 42cm x 125°

FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665014402·

APEX PS Knee

FDA UDI
Omni Life Science, Inc.·00841690113690·PS-C Insert, Size 4 x 20mm

Mariner Outrigger

FDA UDI
Seaspine Orthopedics Corporation·10889981173760·Closed, Axial Rod, Long, 420mm

HITACHI ALTAIRE

FDA 510(k)
FDA Class 2 ·Radiology

PARACON II/FECAL CONCENTRATOR II

FDA 510(k)
FDA Class 1 ·Microbiology

CADD-SOLIS VIP AMBULATORY INFUSION PUMP

FDA Adverse Event
Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·May 1, 2024

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·January 8, 2026

ABG SYRINGE,1 ML LUER-LOK SYRINGE WITH NEEDLE. REGULAR PLUNGER STOPPER &TIP CAP.

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 7, 2017

BD PRESET¿ SYRINGE WITH ATTACHED NEEDLE

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 6, 2017

3 ML BD PRESET¿ SYRINGE WITH BD LUER-LOK¿ TIP. 22 G X 1 IN BD ECLIPSE¿ NEEDLE

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 4, 2017

BD VACUTAINER® SST¿ II ADVANCE PLUS BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 7, 2018

35MM TAP

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·September 24, 2025

35MM TAP

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·January 14, 2025

BD PRESET¿ SYRINGE WITH ATTACHED NEEDLE

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·November 27, 2017

BD PRESET¿ SYRINGE WITH ATTACHED NEEDLE

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 7, 2017

25MM TAP

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·September 24, 2025

25MM TAP

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·June 20, 2025

35MM TAP

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·March 21, 2025