14 results
·
26ms
·
Sources: EU EUDAMED, US FDA
BALLOON RETENTION CHEST CATHETER
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Two Striper
FDA UDI
ABRASIVE TECHNOLOGY, INC.·B868C8020251·Dental Root Canal Post
Arthrex®
FDA UDI
ARTHREX, INC.·10888867042633·5MM CORKSCREW ECONOMY PACK (25)
Alleset
FDA UDI
GRI Medical & Electronic Technology Co., Ltd.·16931918152387·Surgical Gown_Non-Reinforced_L_W/ two hand towe...
BODY-JET
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
RIGID GAS PERMEABLE CONTACT LENS
FDA 510(k)
FDA Class 2
·Ophthalmic
PLATE CDC ANAEROBE 5% SB 100 EA JP
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code JSG·September 9, 2021
PLATE CDC ANAEROBE 5% SB 20 EA
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code JSG·June 28, 2021
SYMBIQ SINGLE CHANNEL
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·February 4, 2014
AUTOMATE 2500 SAMPLE PROCESSING SYSTEM
FDA Adverse Event
Injury
·BECKMAN COULTER, INC.·Product code JQP·October 23, 2012
CARPENTIER-EDWARDS PERIMOUNT MAGNA MITRAL PERICARDIAL BIOPROSTHESIS
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·August 16, 2010
HAMILTON G5
FDA Adverse Event
Malfunction
·HAMILTON MEDICAL AG·Product code CBK·April 2, 2025
PLATE CDC ANAEROBE AGAR 5% SB 90MM 20
FDA Adverse Event
Malfunction
·BECTON DICKINSON GMBH·Product code JSG·February 17, 2022
ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B
FDA Enforcement
Class II
·Ongoing·Siemens Medical Solutions USA, Inc.·February 9, 2022