13 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
PORT-A-CATH LOW PROFILE IMPLANTABLE VENOUS ACCESS SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994869791·DISTRACTOR 2942024 WEDGE DISTRACTOR 18MM
Epimed
FDA UDI
EPIMED INTERNATIONAL, INC·00818788021632·Spirol® 20g x 24" Short Epidural Set
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668110966·STERILIZING CASE 4-KNIVES
NA
FDA UDI
Zimmer, Inc.·00889024454385·
ULTRASONIC LITHOTRIPTOR 300A
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
BRIGHTMATTER NAVIGATION SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
QUANTUM SMART OCCLUDER
FDA Adverse Event
Malfunction
·SPECTRUM MEDICAL LTD·Product code DTQ·January 29, 2025
MEDTRONIC TRANSCATHETER VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·September 27, 2024
ENDOVIVE® STANDARD PEG KIT
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - SPENCER·Product code KNT·February 4, 2013
ACCU-CHEK ® AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·December 30, 2010
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 17, 2014
IMPELLA 5.5
FDA Adverse Event
Death
·ABIOMED, INC.·Product code OZD·September 3, 2025