187 results
·
34ms
·
Sources: EU EUDAMED, US FDA
Filters
Country: United States
×
Relaxis
FDA UDI
Relaxis·00852335007076·Packaged, Relaxis Battery, Medium, Rental
Relaxis
FDA UDI
Relaxis·00852335007069·Packaged, Relaxis Battery, Medium, Refurbished
Relaxis
FDA UDI
Relaxis·00852335007090·Packaged, Relaxis AC, Medium
Relaxis
FDA UDI
Relaxis·00852335007052·Packaged, Relaxis Battery, Medium
Relaxis
FDA UDI
Relaxis·00852335007038·Packaged, Relaxis AC, Medium, Rental
Relaxis
FDA UDI
Relaxis·00852335007021·Packaged, Relaxis AC, Medium, Refurbished
Relaxis
FDA UDI
Relaxis·00852335007083·Replacement Power Supply, Relaxis
RELAXY-WONDER KNOCK
FDA 510(k)
FDA Class 1
·Physical Medicine
RELAXY-THE WONDER HAND
FDA 510(k)
FDA Class 1
·Physical Medicine
MRI MAGNET RADIOLOGY INSTRUMENT
FDA Adverse Event
Injury
·Product code LNH·March 26, 2017
ICY HOT HEAT THERAPY
FDA Adverse Event
Injury
·CHATTEM·Product code IMD·February 19, 2008
Etac Relax wall mounted shower seat The Etac Relax is a wall mounted shower seat designed as a seating and standing support for personal hygiene purposes for people with reduced mobility. The Etac Relax shower seat is used for sitting where space is restricted, and can be folded up when not in use. Etac Relax is intended for home use.
FDA Recall
Terminated
·Etac Supply Center Ab Langgatan 12 Anderstorp Sweden·Product code ILS·July 12, 2015
POWERPICC PROVENA 3F SL MBPLUS (3CG, BIOPATCH, PROBE COVER)
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (BASD) -3006260740·Product code LJS·August 13, 2024
POWERPICC PROVENA 3F SL MBPLUS (3CG, BIOPATCH, PROBE COVER)
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (BASD) -3006260740·Product code LJS·August 13, 2024
BARD ACCUCATH MIDLINE CATHETER
FDA Adverse Event
Malfunction
·BARD ACCESS SYSTEMS·Product code FOZ·July 3, 2019
DORNIER RELAX + TABLE
FDA Adverse Event
Injury
·DORNIER MEDTECH SYSTEM GMBH·Product code LNS·July 14, 2015
DORNIER RELAX+ TABLE
FDA Adverse Event
Malfunction
·DORNIER MEDTECH AMERICA, INC.·Product code LNS·January 6, 2011
DORNIER RELAX + TABLE
FDA Adverse Event
Malfunction
·DORNIER MEDTECH SYSTEMS GMBH·Product code KQS·November 6, 2012
DORNIER RELAX + TABLE
FDA Adverse Event
Injury
·DORNIER MEDTECH SYSTEMS GMBH·Product code LNS·March 4, 2019
DORNIER RELAX+ TABLE
FDA Adverse Event
Injury
·DORNIER MEDTECH SYSTEMS GMBH·Product code LNS·April 30, 2015