61 results · 21ms · Sources: EU EUDAMED, US FDA

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MEDELA VARIO 8/18/CI SECRETION & SURGICAL ASPIRATOR

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

DP-REPAIR

FDA UDI
Denplus Inc·D8451061205·DP-REPAIR-R, LPI, 2.3 kg

SuperNova

FDA UDI
PURELIFE, LLC·D79010612051·SuperNova Nitrile Powder-Free, X-Large, Revolut...

BioQuick®

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR70612051·BioQuick-Brackets FACE Evolution II System .018...

CosmoLock Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07311K0112050·Tap, 7.5 mm

Waterpik Wizard Wedges

FDA UDI
WATER PIK, INC.·D6860612050003·Wood matrix wedges, assortment of sizes - 25 ea...

ISOAID IODINE BRACHTHERAPY SEEDS, MODEL ADVANTAGE I-125

FDA 510(k)
FDA Class 2 ·Radiology

PASCO MIC AND MIC/ID PANELS

FDA 510(k)
FDA Class 2 ·Microbiology

CT/MR Fletcher (FSD) IU Tube, 6.0cm, Varian

FDA UDI
MICK RADIO NUCLEAR INSTRUMENT, INC·00817330021328·

CT/MR Fletcher (FSD) IU Tube, 8.0cm, Varian

FDA UDI
MICK RADIO NUCLEAR INSTRUMENT, INC·00817330021335·

CT/MR Fletcher (FSD) IU Tube, 2.0cm, Varian

FDA UDI
MICK RADIO NUCLEAR INSTRUMENT, INC·00817330027603·

CT/MR Fletcher (FSD) IU Tube, 4.0cm, Varian

FDA UDI
MICK RADIO NUCLEAR INSTRUMENT, INC·00817330021311·

CT/MR Fletcher (FSD) IU Tube, 6.0cm, Varian

FDA UDI
MICK RADIO NUCLEAR INSTRUMENT, INC·00817330021373·

CT/MR Fletcher (FSD) IU Tube, 8.0cm, Varian

FDA UDI
MICK RADIO NUCLEAR INSTRUMENT, INC·00817330021380·

VACUETTE

FDA Adverse Event
Malfunction ·GREINER BIO-ONE NORTH AMERICA·Product code JKA·August 7, 2012

C-T II PORT CLOSURE, 10/15 (MM)

FDA Adverse Event
Malfunction ·COOPERSURGICAL, INC.·Product code KOH·April 10, 2013

530G INSULIN PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OZO·September 4, 2014

LOANER - US, PUMP,COLLEAGUESINGLE CHANNEL COLOUR

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·April 18, 2011

BD SMARTSITE¿ NEEDLE-FREE CONNECTOR

FDA Adverse Event
Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·June 13, 2022

SIGMA HP UNI FB KEEL OSTEOTOME

FDA Adverse Event
Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code HWM·March 18, 2017