187 results · 34ms · Sources: EU EUDAMED, US FDA

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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