61 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
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