25 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K1100530·Caddie, 7.5mm Screws
CORRECTINJECT SAFETY SYSTEM, CATHETER CONNECTOR, FILTER, INFUSION ADAPTOR, SYRINGE KIT
FDA 510(k)
FDA Class 2
·Anesthesiology
Corin BiPolar-i
FDA UDI
CORIN LTD·05056139233999·Acetabular Trial Ø53
OsteoMed
FDA UDI
OSTEOMED LLC·00845694055239·3mm Short Pituitary Rongeur, Straight
MATTIOLI PULSE TWO/THREE PLUS FAMILY
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HUMI-FLOW, MODEL 6-850-00/ 01/02
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
RESPIRONICS
FDA Adverse Event
Malfunction
·Product code MNT·April 8, 2021
MG II®
FDA UDI
Zimmer, Inc.·00889024436039·
MG II®
FDA UDI
Zimmer, Inc.·00889024436053·
MG II®
FDA UDI
Zimmer, Inc.·00889024436022·
MG II®
FDA UDI
Zimmer, Inc.·00889024436015·
MG II®
FDA UDI
Zimmer, Inc.·00889024582699·
MG II®
FDA UDI
Zimmer, Inc.·00889024436060·
MG II®
FDA UDI
Zimmer, Inc.·00889024436046·
UNKNOWN MICROCATHETER
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code DQY·May 30, 2017
INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR
FDA Adverse Event
Injury
·MSD DEGGENDORF MFG·Product code OVD·December 18, 2019
PIPELINE EMBOLIZATION DEVICE
FDA Adverse Event
Injury
·EV3 NEUROVASCULAR·Product code OUT·May 13, 2013
PLUM A+ DRIVER EDITI
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·September 11, 2014
RADIAL ARTERY CATHETERIZATION SET
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL·Product code DQY·May 20, 2011
SS 3.5MM Diamond Tip Trocar - Medium Gloves Catalog Number: B1555
FDA Enforcement
Class II
·Terminated·Busse Hospital Disposables, Inc.·June 8, 2022