10,000 results
·
40ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
NA
FDA UDI
Fehling Instruments GmbH & Co. KG·04058749048018·MITHOS Lung grasping clamp cvd. 11x340mm, shaft...
NA
FDA UDI
Fehling Instruments GmbH & Co. KG·04058749047998·MITHOS Lung grasping clamp cvd., 12 x 350 mm, s...
OT EQUATOR - OT BRIDGE
FDA UDI
RHEIN 83 SRL·08059224139869·Straight Titanium abutment H 3mm with passing h...
OT EQUATOR-OT BRIDGE
FDA UDI
RHEIN 83 SRL·D821MTE100·
MTE-T RADIOGRPHIC/TOMOGRAPHIC ELEVATING TABLE
FDA 510(k)
FDA Class 2
·Radiology
VITEK® 2 ANC TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC·Product code JSP·August 5, 2016
DISPOSABLE BLOOD PRESSURE CUFF
FDA Adverse Event
Malfunction
·MEDLINE INDUSTRIES, INC.·Product code DXQ·November 30, 2023
O-ARM 1000 IMAGING SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·July 25, 2016
INFUSOMAT
FDA Adverse Event
Injury
·B. BRAUN MEDICAL INC.·Product code FRN·December 5, 2024
VITEK® 2 NH ID TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX INC.·Product code JST·August 18, 2017
VALVE SET, EM2400
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code LHI·June 13, 2022
VISUALASE LASER GUIDED ABLATION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC NAVIGATION, INC·Product code GEX·May 2, 2019
VISUALASE LASER GUIDED ABLATION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC NAVIGATION, INC·Product code GEX·May 2, 2019
O-ARM O2 IMAGING SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OWB·June 1, 2018
INFUSOMAT®
FDA Adverse Event
Malfunction
·B. BRAUN AVITUM AG·Product code FRN·December 5, 2024
CURRENT VR RF CD-1211-36Q
FDA Adverse Event
Injury
·ST JUDE·Product code MTE·January 26, 2010
SYSTEM, PACING, TEMPORARY, ACUTE, INTERNAL ATRIAL DEFIBRILLATION
FDA Adverse Event
Malfunction
·ZOLL MEDICAL·Product code MTE·April 30, 2021
ELECTROPHYSIOLOGY (FIXED)
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.·Product code MTE·January 18, 2017
IBI¿ 1400-CV CARDIOVERSION II SWITCH BOX
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.·Product code MTE·February 7, 2019
ALERT INTERNAL CARDIOVERSION CATHETER
FDA Adverse Event
Death
·DOT MEDICAL PRODUCTS LTD·Product code MTE·April 24, 2017