3,128 results
·
30ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
NeoConnect Oral Administration Tip
FDA UDI
NEOMED, INC.·00817584011038·NeoConnect DoseMate, Oral Administration Tip, S...
NEOMED*
FDA UDI
Avanos Medical, Inc.·00350770000466·ENFit DoseMate Sterile Purp
NeoConnect DoseMate DL Oral Administration Tip
FDA UDI
NEOMED, INC.·00817584013100·NeoConnect DoseMate Long, Oral Administration T...
NEOMED*
FDA UDI
Avanos Medical, Inc.·00350770000473·ENFit DoseMate DL Sterile Purp
Bluegrass, Kentucky/June Poa pratensis
FDA UDI
HYCOR BIOMEDICAL LLC·00816879021431·A substance or reactant intended to be used tog...
NOVEOS Kentucky Blue Grass, Poa pratensis
FDA UDI
HYCOR BIOMEDICAL LLC·00816879029307·
OXYGEN SUPPLY TUBE 25'
FDA Adverse Event
Death
·SUNSET·Product code CAT·June 21, 2018
MALLINCKRODT
FDA Adverse Event
Death
·COVIDIEN·Product code BTR·June 18, 2008
LIBERTY CYCLER
FDA Adverse Event
Injury
·CONCORD MANUFACTURING·Product code FKX·July 8, 2017
MED COMP
FDA Adverse Event
Malfunction
·MED COMP·Product code MSD·November 25, 2002
IN.PACT ADMIRAL PACLITAXEL-ELUTING PTA BALLOON CATHETER
FDA Adverse Event
Injury
·INVATEC TECHNOLOGY CENTER GMBH·Product code ONU·October 2, 2015
IN.PACT ADMIRAL PACLITAXEL-ELUTING PTA BALLOON CATHETER
FDA Adverse Event
Injury
·INVATEC TECHNOLOGY CENTER GMBH·Product code ONU·October 2, 2015
IN.PACT ADMIRAL PACLITAXEL-ELUTING PTA BALLOON CATHETER
FDA Adverse Event
Injury
·INVATEC TECHNOLOGY CENTER GMBH·Product code ONU·October 2, 2015
TWO-LUMEN CENTRAL VENOUS CATHETERIZATION KIT WITH BLUE FLEXT
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL, A SUBSIDIARY OFTELEFLEX INC.·Product code FOZ·February 13, 2014
NOVEOS Capture Reagent Pack Kentucky Blue Grass, Poa pratensis
FDA UDI
HYCOR BIOMEDICAL LLC·00816879025255·
V-GO DISPOSABLE INSULIN DELIVERY DEVICE
FDA Adverse Event
Malfunction
·VALERITAS, INC.·Product code LZG·March 24, 2020
BD FACSLYRIC¿
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code OYE·August 17, 2022
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL MANUFACTURING CORPORATION·Product code MVK·November 17, 2025
V-GO DISPOSABLE INSULIN DELIVERY DEVICE
FDA Adverse Event
Injury
·ZEALAND PHARMA U.S. INC.·Product code LZG·April 28, 2022
CYPHER OTW
FDA Adverse Event
Injury
·CORDIS CORP·Product code NIQ·May 24, 2004