725 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MERSILENE TAPE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code KDC·March 5, 2019
HARMONIC ACE 5MM SHEAR
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·July 1, 2025
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·April 9, 2018
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·January 25, 2013
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·January 25, 2013
ImagePilot, Model No. D9MA
FDA Recall
Terminated
·Konica Minolta Medical Imaging USA, Inc.·Product code LLZ·May 9, 2018
CS-7, Model No. A4C1
FDA Recall
Terminated
·Konica Minolta Medical Imaging USA, Inc.·Product code MQB·May 9, 2018
Ige, Peroxidase, Antigen, Antiserum, Control
FDA classification
FDA Class 2
·Ige, Peroxidase, Antigen, Antiserum, Control
ROLAND DGA
FDA registration
ROLAND DGA·1 product·🇺🇸 United States
NEONATAL TRANSPAC IV MONITORING KITS
FDA Adverse Event
Other
·ICU MEDICAL, INC.·Product code DRS·December 22, 2011
FLOW-I C30
FDA Adverse Event
Malfunction
·MAQUET CRITICAL CARE AB·Product code BSZ·May 7, 2014
ELEGANCE - DEO, MODIFICATION
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
ADJUSTRETTE - DAO, MODIFICATION
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
PEACH 2 go
FDA UDI
Foreo AB·07350120791900·PEACH™ 2 go is an over-the-counter device inten...
BEAR 2 go
FDA UDI
Foreo AB·07350120791849·Bear 2 go is intended for facial and neck stimu...
SAMBA 2 GO
FDA UDI
Med-El Elektromedizinische Geräte Gesellschaft m.b.H.·09008737525071·Audio Processor Streaming Device
PEACH 2 go
FDA UDI
Foreo AB·07350120791917·PEACH™ 2 go is an over-the-counter device inten...
BEAR 2 go
FDA UDI
Foreo AB·07350120791825·Bear 2 go is intended for facial and neck stimu...
PEACH 2 go
FDA UDI
Foreo AB·07350120791894·PEACH 2 go is an over-the-counter device intend...
Freemie
FDA UDI
DAO HEALTH·00851690007257·32mm Single Cone Spare Part