50 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SYNTHES (USA) DISTRACTION OSTEOGENESIS SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
BLESSINGS SCISSORS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896011380·BLESSING SCISSORS TUNGSTEN CARBIDE CURVED TIP
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702467697·Elvarex 3/Knee High/Profile-Slant-Closed Toe-El...
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702261509·Elvarex Forte 3/Thigh High/Slant, Closed Toe, E...
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702590661·Elvarex 1/Knee High/Profile-Slant-Closed Toe/So...
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702293791·Elvarex 3/Thigh High/Slant-Open Toe-Elephantias...
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702445831·Elvarex Forte 3/Knee High/Slant-Closed Toe-Elep...
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702457728·Elvarex 2/Knee High/Slant-Open Toe/Dotted 5 cm ...
<GENX> CODA INCUBATOR CELLMATE
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
CONDUCTION CATHETER
FDA 510(k)
FDA Class 2
·General Hospital
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTEC)·Product code NEW·November 14, 2008
ARROW PI CVC KIT: 3L 7 FR X 16 CM AGB
FDA Adverse Event
Injury
·ARROW INTERNATIONAL LLC·Product code FOZ·November 12, 2025
BD SYRINGE 5 ML S/T BNS
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·February 4, 2023
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code NEW·June 18, 2010
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES (DBA ANGIOTECH)·Product code NEW·March 28, 2008
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 30, 2009
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 30, 2009
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code ITI·April 10, 2013
CAPSUREFIX
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·April 12, 2011
GUIDANT TW POWER SUPPLY, US
FDA Adverse Event
Malfunction
·GUIDANT CARDIAC SURGERY·Product code GEI·May 19, 2008