45 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IMPAX VOLUME VIEWING 3.0
FDA 510(k)
FDA Class 2
·Radiology
NA
FDA UDI
MEDTRONIC XOMED, INC.·00681490034531·PROSTHESIS 1133135 CUP STAPES .6X4.0 SST
Per-Q-Cath Plus Midline Catheter
FDA UDI
Bard Access Systems, Inc.·00801741074868·Per-Q-Cath Plus Midline Catheter 3F Single-Lume...
STRYKER WIRELESS UNIVERSAL FOOTSWITCH SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
UNISTRIP 1
FDA 510(k)
FDA Class 2
·Clinical Chemistry
PULSE GEN MODEL UNK
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code LYJ·February 10, 2009
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·October 6, 2022
T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code OZO·June 30, 2022
NAIL, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code JDW·July 22, 2016
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·December 4, 2020
ENDOTAK RELIANCE
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVY·January 15, 2016
INCEPTA
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·January 15, 2016
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·July 22, 2016
BIPOL LEAD MODEL 300
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code LYJ·August 21, 2008
BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B LABORATORY KIT
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·March 3, 2026
ELECSYS 2010 RACK
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·May 26, 2009
PROTECTA XT CRT-D
FDA Adverse Event
Death
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·May 29, 2013
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FKX·October 1, 2014
SPRINT QUATTRO SECURE
FDA Adverse Event
Malfunction
·MPRI·Product code LWS·October 7, 2015
ARCHITECT C4000
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code JJE·April 30, 2024