10 results
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54ms
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Sources: EU EUDAMED, US FDA
CLARITY DESIGN, INC.
FDA registration
CLARITY DESIGN, INC.·3 products·🇺🇸 United States
BD BBL¿ THIOGLYCOLLATE MEDIUM WITHOUT INDICATOR
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code JSG·May 16, 2023
SNOWDEN PENCER
FDA Adverse Event
Other
·CAREFUSION 2200, INC.·Product code GEI·March 29, 2024
LIGHTMAT ULTRA-THIN FLEXIBLE SURGICAL ILLUMINATOR
FDA Adverse Event
Other
·LUMITEX·Product code HJN·July 3, 2008
CONFIRM ANTI-HER-2/NEU (4B5) PRIMARY ANTIBODY
FDA Adverse Event
Other
·VENTANA MEDICAL SYSTEMS, INC.·Product code MVC·March 20, 2012
TECNIS ODYSSEY TORIC II IOL
FDA Adverse Event
Injury
·AMO MANUFACTURING NETHERLANDS·Product code MFK·June 27, 2025
Psephos Limited
Authorized representative
🇮🇪 Ireland·13 Manufacturers·26 Devices
Plum A+ Hyperbaric Single Channel Infusion Pumps with Hospira MedNet Software and a Connectivity Engine peripheral module that provides wired Ethernet and wireless local networking, allowing the MedNet software to download drug libraries to the infuser and enable the auto-programming feature; Hospira, Inc., Lake Forest, IL 60045; pump list number 11005, module list number 11006 Product Usage: The Plum A+ Hyperbaric Infusion System is exclusively designed for hyperbaric therapy in monospace and multiplace chambers.
FDA Recall
Terminated
·Hospira Inc.·Product code FRN·October 26, 2012
Medtronic Intersept Custom Tubing Pack, which are designed as specified by the user. The following models contain a Pressure Display Set. Sterilized by Ethylene Oxide. Non-pyrogenic. Manufacturer: Medtronic, Inc. 710 Medtronic Parkway, Minneapolis, MN 55432-5604. Product Usage: This product is intended for use in monitoring catheter, cannula, or line pressures associated with cardiopulmonary bypass equipment and/or related products.
FDA Recall
Terminated
·Medtronic Perfusion Systems·Product code DXS·September 9, 2011
European Healthcare & Device Solutions Ltd.
Authorized representative
🇮🇪 Ireland·66 Manufacturers·867 Devices