49 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MAGNETOM Aera and MAGNETOM Skyra with syngo MR E11C - AP02 Software
FDA 510(k)
FDA Class 2
·Radiology
Archimed 631 Spinal Brace
FDA UDI
MEDICAL SPECIALTIES INCORPORATED·00802357633128·
Laparoscope
FDA UDI
SOPRO-COMEG GmbH·04059082032313·
Laparoscope
FDA UDI
SOPRO-COMEG GmbH·04059082003849·
Laparoscope
FDA UDI
SOPRO-COMEG GmbH·04059082003832·
Laparoscope
FDA UDI
SOPRO-COMEG GmbH·04059082032306·
N.A.
FDA UDI
DENTAURUM GmbH & Co.KG·J011163312000·ConTec Go! etching gel in syringes
UPD-Y0003
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MODIFICATION TO ATLANTIS SR PRO 2 AND SR PRO CORONARY IMAGING CATHETERS, MODEL 39014 AND 38942
FDA 510(k)
FDA Class 2
·Cardiovascular
UNKNOWN HIP
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JDI·February 3, 2017
UNKNOWN HIP
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JDI·February 2, 2017
UNKNOW HIP
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JDI·February 3, 2017
PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code NEW·December 3, 2019
PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAW·December 3, 2019
KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LOX·March 17, 2020
UNKNOWN HIP
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JDI·February 2, 2017
UNKNOWN HIP
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JDG·February 3, 2017
GYNECARE TVT OBURATOR SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·June 11, 2013
ALTRUA
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 15, 2011
TOTALCARE BARIATRIC
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·September 9, 2008