335 results · 24ms · Sources: EU EUDAMED, US FDA

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Préime DermaFacial (MicroT)

FDA 510(k)
FDA Class 2 ·Neurology

Oph. Cystotomes

FDA UDI
KATENA PRODUCTS, INC.·00841668113721·CYSTOTOME CURVED 27GA

BECTON DICKINSON

FDA registration
BECTON DICKINSON·52 products·🇺🇸 United States

BD NEEDLE

FDA Adverse Event
Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMI·May 28, 2026

GEN-PROBE APTIMA ASSAY FOR CHLAMYDIA TRACHOMATIS

FDA 510(k)
FDA Class 1 ·Microbiology

ENROUTE Transcarotid Neuroprotection System

FDA 510(k)
FDA Class 2 ·Cardiovascular

BD PLASTIPAK SYRINGES

FDA Adverse Event
Injury ·BECTON DICKINSON·Product code FMF·March 15, 2013

BD PLASTIPAK SYRINGES

FDA Adverse Event
Injury ·BECTON DICKINSON·Product code FMF·March 15, 2013

BD PLASTIPAK SYRINGES

FDA Adverse Event
Injury ·BECTON DICKINSON·Product code FMF·March 15, 2013

BD PLASTIPAK SYRINGES

FDA Adverse Event
Injury ·BECTON DICKINSON·Product code FMF·March 15, 2013

ECLIPSE LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMI·March 30, 2026

VENFLON 2 BL 22GA IV CANNULA

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FOZ·December 24, 2020

BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE

FDA Adverse Event
Malfunction ·BD CARIBE LTD.·Product code JKA·February 12, 2025

BD¿ SHARPS COLLECTOR

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMI·June 16, 2023

2243072-2017-00211

FDA Adverse Event
Malfunction ·October 27, 2017

2243072-2017-00238

FDA Adverse Event
Malfunction ·December 1, 2017

2243072-2017-00228

FDA Adverse Event
Injury ·December 1, 2017

2243072-2017-00209

FDA Adverse Event
Malfunction ·October 31, 2017

2243072-2017-00413

FDA Adverse Event
Malfunction ·December 28, 2017

2243072-2017-00197

FDA Adverse Event
Malfunction ·October 30, 2017