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

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Hyaluronic Acid Vaginal Suppository (HA 5 mg); Hyaluronic Acid Vaginal Suppository (HA 10 mg)

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

SWANSON

FDA UDI
WRIGHT MEDICAL TECHNOLOGY, INC.·00840420121509·

Humelock II Cemented Shoulder System

FDA UDI
FX SOLUTIONS·03701037304723·HUMELOCK II TRIAL STEM T07

NA

FDA UDI
Stryker Leibinger GmbH & Co. KG·07613154546336·DRILL, F. 6+7MM SCREWS, STRYKER SHAFT

Mini Cradle with Splitter - US

FDA UDI
EITAN MEDICAL LTD·17290109154029·

Mini Cradle with Splitter- US

FDA UDI
EITAN MEDICAL LTD·17290109150014·

Mini Cradle with Splitter- US

FDA UDI
EITAN MEDICAL LTD·17290109150113·

BD AUTOSHIELD PEN NEEDLE

FDA 510(k)
FDA Class 2 ·General Hospital

Paclitaxel Sets

FDA 510(k)
FDA Class 2 ·General Hospital

Trilogy®

FDA UDI
Zimmer, Inc.·00889024119949·

Trilogy®

FDA UDI
Zimmer, Inc.·00889024119956·

CLEARLINK PACLITAXEL SETS

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·February 2, 2024

CLEARLINK SOLUTION ADMINISTRATION SETS

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·April 27, 2022

CLEARLINK SOLUTION ADMINISTRATION SETS

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·April 27, 2022

UNKNOWN DEPUY INSERT

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HSH·December 9, 2008

COLLEAGUE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 22, 2011

HILL-ROM

FDA Adverse Event
Other ·HILL ROM·Product code FNL·July 26, 2013

BD INSULIN PEN NEEDLE

FDA Adverse Event
Injury ·BECTON DICKINSON AND CO.·Product code FMI·November 9, 2015

Cyberonics VNS Therapy AspireHC Model 105 Generator, 26-0007-4000/3. The firm name on the label is CYBERONICS, INC., Houston, TX. Vagus nerve stimulator.

FDA Recall
Terminated ·LivaNova USA Inc·Product code LYJ·November 16, 2018

Cyberonics VNS Therapy AspireSR, Model 106 Generator, 26-0007-8400/1. The firm name on the label is CYBERONICS, INC., Houston, TX. Vagus nerve stimulator.

FDA Recall
Terminated ·LivaNova USA Inc·Product code LYJ·November 16, 2018