74 results
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31ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SPLASH! IMPRESSION MATERIAL DEVICE
FDA 510(k)
FDA Class 2
·Dental
Armada
FDA UDI
Nuvasive, Inc.·00887517208675·ARM15T Rod, 90mm Conventional Pre-Bent
I-neb
FDA UDI
RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD·00383730003634·I-neb CF Chamber Assembly Tobramycin.
CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SYNTEX PRE-POWDERED NITRILE EXAMINATION GLOVE
FDA 510(k)
FDA Class 1
·General Hospital
ARCHITECT CA19-9XR
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·October 31, 2025
ALINITY I CA 19-9XR REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·May 19, 2026
TAXUS¿ ELEMENT¿
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·April 11, 2013
TERUMO CDI 540 CALIBRATOR
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·March 1, 2011
BIOMET CC CRUCIATE TRAY
FDA Adverse Event
Malfunction
·BIOMET, INC.·Product code JWH·May 20, 2008
ALINITY I CA 19-9XR REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·May 1, 2026
QUIK-COMBO PACING/DEFIBRILLATION/ECG
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL CORP·Product code LDD·March 31, 1998
ALINITY I CA 19-9XR REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·May 14, 2026
TPRLC 133 FP TYPE1 PPS SO 4.0
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code LPH·February 21, 2020
TPRLC 133 FP TYPE1 PPS SO 4.0
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code LPH·February 21, 2020
TPRLC 133 T1 PPS HO 9X137MM MM T1
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code KWA·February 21, 2020
TPRLC 133 T1 PPS HO 13X146MM 6MM T1
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code KWA·February 21, 2020
TPRLC XR T1 PPS 17X154MM MM T1
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code LPH·February 21, 2020
ALINITY I CA 19-9XR REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·December 9, 2025
ARCHITECT CA19-9XR
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·December 22, 2025