245 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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VITREA CT TRANSCATHETER AORTIC VALVE REPLACMENT (TAVR) PLANNING
FDA 510(k)
FDA Class 2
·Radiology
ACE
FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950024230·PROBE LACRIMAL BOWMAN STERLING SIZE 7-8 5" 13CM...
APEX PS KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ENDIUS FLEXTIP BLADE
FDA 510(k)
FDA Class 2
·Orthopedic
ULTRASAFE X100L PNG CLEAR NVS STEIN
FDA Adverse Event
Malfunction
·BECTON DICKINSON HUNGARY KFT (BD)·Product code MEG·February 5, 2021
ULTRASAFE X100L PNG RASPBERRY NVS STEIN
FDA Adverse Event
Malfunction
·BECTON DICKINSON HUNGARY KFT (BD)·Product code MEG·February 10, 2020
SOLETRA
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·May 21, 2013
ADVANCE(R) TOT COND FEMORAL NON-POROUS
FDA Adverse Event
Injury
·MICROPORT ORTHOPEDICS INC.·Product code JWH·September 26, 2014
SPRINT FIDELIS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·June 14, 2011
ULTRASAFE X100L PNG RASPBERRY NVS STEIN
FDA Adverse Event
Malfunction
·BECTON DICKINSON HUNGARY KFT (BD)·Product code MEG·January 26, 2021
BD ULTRASAFE X100L PR CLEAR SSL NVS STEIN
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code MEG·July 26, 2019
1) Accolade II 127 Neck Angle Hip Stem, Size # 3 2) Accolade II 127 Neck Angle Hip Stem, Size #5 Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430 USA Telephone # +1 201-831-5000 Stryker France ZAC Satolas Green Pusignan Av de Satolas Green 69881 MEYZIEU Cedex France Intended for cementless application in total or hemiarthroplasty procedures.
FDA Enforcement
Class II
·Terminated·Stryker Howmedica Osteonics Corp.·December 18, 2013
BD ULTRASAFE PASSIVE¿ X-SERIES NEEDLE GUARD SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON HUNGARY KFT (BD)·Product code MEG·September 19, 2018
ULTRASAFE X100L PNG CLEAR NVS STEIN
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code MEG·September 24, 2019
ULTRASAFE X100L PR PLUM SSL NVS STEIN
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code MEG·September 26, 2019
SCREW, UNKNOWN TYPE
FDA Adverse Event
Malfunction
·ZIMMER BIOMET SPINE INC.·Product code KWP·June 17, 2019
ULTRASAFE X100L PNG RASPBERRY NVS STEIN
FDA Adverse Event
Malfunction
·BECTON DICKINSON HUNGARY KFT (BD)·Product code MEG·March 19, 2019
SCREW, UNKNOWN TYPE
FDA Adverse Event
Malfunction
·ZIMMER BIOMET SPINE INC.·Product code KWP·June 17, 2019
BD ULTRASAFE PASSIVE X-SERIES NEEDLE GUARD SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON HUNGARY KFT (BD)·Product code MEG·February 27, 2020
ULTRASAFE X100L PNG CLEAR NVS STEIN
FDA Adverse Event
Malfunction
·BECTON DICKINSON HUNGARY KFT (BD)·Product code MEG·March 27, 2021