24 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Alpha Pure
FDA 510(k)
FDA Class 2
·Dental
PILLING
FDA UDI
TELEFLEX INCORPORATED·24026704509151·
Portex
FDA UDI
ICU MEDICAL, INC.·00351688034918·
N.A.
FDA UDI
DENTAURUM GmbH & Co.KG·J0111631170000·CONTEC disposable brush for adhesives
MODIFICATION TO DUREPAIR DURA REGENERATION MATRIX
FDA 510(k)
FDA Class 2
·Neurology
ITOTAL CRUCIATE RETAINING (CR) KNEE REPLACEMENT SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
OT VERIO FLEX METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE GMBH·Product code NBW·May 21, 2019
WRIST BLOOD PRESSURE UNIT
FDA Adverse Event
Malfunction
·MEDLINE INDUSTRIES, LP - NORTHFIELD·Product code DXN·July 12, 2022
STEM: AMISTEM C CEMENTED STD SIZE 2
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·February 3, 2021
IMPAX CV REPORTING
FDA Adverse Event
Malfunction
·AGFA HEALTHCARE CORP.·Product code LLZ·June 11, 2013
ESPRIT VENTILATOR
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, INC.·Product code CBK·July 15, 2011
TRIDENT HEMISPHERICAL CLUSTER 58MM
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS CORK·Product code MEH·September 16, 2008
COOK® SINGLE-USE HOLMIUM LASER FIBER
FDA Adverse Event
Malfunction
·COOK INC·Product code GEX·May 17, 2019
COOK® SINGLE-USE HOLMIUM LASER FIBER
FDA Adverse Event
Malfunction
·COOK INC·Product code GEX·March 18, 2019
OPTILITE SINGLE-USE HOLMIUM LASER FIBER
FDA Adverse Event
Malfunction
·COOK INC·Product code GEX·June 5, 2020
COOK® SINGLE-USE HOLMIUM LASER FIBER
FDA Adverse Event
Malfunction
·COOK INC·Product code GEX·March 12, 2019
COOK® SINGLE-USE HOLMIUM LASER FIBER
FDA Adverse Event
Malfunction
·COOK INC·Product code GEX·March 18, 2019
COOK® SINGLE-USE HOLMIUM LASER FIBER
FDA Adverse Event
Injury
·COOK INC·Product code GEX·November 4, 2022
OPTILITE SINGLE-USE HOLMIUM LASER FIBER
FDA Adverse Event
Malfunction
·COOK INC·Product code GEX·February 13, 2020
NIPRO BLOOD TUBING SET W/TRANSDUCER PROTECTOR
FDA Adverse Event
Injury
·NIPRO (THAILAND) CORP., LTD.·Product code FJK·March 16, 2018