26 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CLEARCUT S SAFETY KNIFE
FDA 510(k)
FDA Class 1
·Ophthalmic
Leva® Anterior Interbody System
FDA UDI
Spine Wave, Inc.·10840642108804·Modular Spacer, SSA, 26 mm (W) x 26 mm (L) x 15...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450160145·
4D-VIEW 9.1 (4D VIEW PC SOFTWARE) MODEL: H48651SZ
FDA 510(k)
FDA Class 2
·Radiology
IMAGYN ISOSLEEVE / ISOSTAR NEEDLE SYSTEM
FDA 510(k)
FDA Class 1
·Radiology
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·October 6, 2023
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·November 9, 2023
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 7, 2025
QUICK CHECK ONE
FDA Adverse Event
DIAGNOSTIC SOLUTIONS, INC.·Product code CFR·April 10, 1997
QUICK CHECK ONE
FDA Adverse Event
DIAGNOSTIC SOLUTIONS, INC.·Product code CFR·March 17, 1997
ATTUNE FB TIB BASE SZ 4 CEM
FDA Adverse Event
Injury
·DEPUY IRELAND - 9616671·Product code JWH·October 16, 2019
MAXCEM ELITE
FDA Adverse Event
Malfunction
·KERR CORPORATION·Product code EMA·May 13, 2013
QC F/K-WIRES Ø0.6-3.2 F/532.001 532.010
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HWE·September 23, 2014
M2A MODULAR HEAD COMPONENT 38MM HEAD DIAMETER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·June 1, 2011
PEDIASAT
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES PR·Product code DRE·December 10, 2025
EDWARDS OXIMETRY CENTRAL VENOUS CATHETER
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES·Product code DXG·January 7, 2025
EDWARDS OXIMETRY CENTRAL VENOUS CATHETER
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES PR·Product code DQE·March 27, 2025
EDWARDS OXIMETRY CENTRAL VENOUS CATHETER
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES·Product code DXG·January 7, 2025
QUICK CHECK ONE
FDA Adverse Event
DIAGNOSTIC SOLUTIONS, INC.·Product code CFR·April 17, 1997
DEKA SMARTXIDE² TRIO
FDA Adverse Event
Malfunction
·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·October 31, 2023