10,000 results
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57ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Phoenix Elastics
FDA UDI
PHOENIX ORTHODONTICS INC·05060772892680·LATEX NEON GREEN E 3-8 MEDIUM 3.5 OZ ELASTICS 1...
NGage
FDA UDI
COOK INCORPORATED·00827002482944·NGage, Nitinol Stone Extractor
NGage
FDA UDI
COOK INCORPORATED·00827002482975·NGage, Nitinol Stone Extractor
NGage
FDA UDI
COOK INCORPORATED·00827002482951·NGage, Nitinol Stone Extractor Modified Basket
NGage
FDA UDI
COOK INCORPORATED·00827002482968·NGage Nitinol Stone Extractor Modified Basket
UNK LINX MAGNETIC IMPLANT
FDA Adverse Event
Injury
·TORAX MEDICAL, INC.·Product code LEI·April 10, 2024
NGAGE NITINOL STONE EXTRACTOR
FDA Adverse Event
Malfunction
·COOK INC·Product code FFL·February 10, 2020
NGAGE NITINOL STONE EXTRACTOR
FDA Adverse Event
Malfunction
·COOK INC·Product code FFL·August 18, 2023
NGAGE NITINOL STONE EXTRACTOR
FDA Adverse Event
Malfunction
·COOK INC·Product code FFL·August 15, 2023
NGAGE NITINOL STONE EXTRACTOR
FDA Adverse Event
Malfunction
·COOK INC·Product code FFL·March 27, 2023
SURGIPRO* 4/0 36 BLUE CV-25 D/A
FDA Adverse Event
Injury
·COVIDIEN·Product code GAW·January 28, 2015
OVU-QUICK ONE-STEP
FDA Adverse Event
Malfunction
·QUIDEL CORP·Product code NGE·October 20, 2003
INITO FERTILITY MONITOR
FDA Adverse Event
Malfunction
·CENTUM ELECTRONICS LIMITED·Product code NGE·September 5, 2024
INITO FERTILITY MONITOR
FDA Adverse Event
Malfunction
·CENTUM ELECTRONICS LIMITED·Product code NGE·December 29, 2025
INITO HORMONE MONITOR
FDA Adverse Event
Malfunction
·INITO LLC / INITO HEALTH TECH PRIVATE LIMITED·Product code NGE·December 18, 2025
INITO FERTILITY MONITOR
FDA Adverse Event
Malfunction
·CENTUM ELECTRONICS LIMITED·Product code NGE·December 22, 2022
UP AND UP OVULATION TEST
FDA Adverse Event
Malfunction
·MFR UNK·Product code NGE·June 3, 2017
SURESCAN
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·July 28, 2015
SPRINT QUATTRO SECURE S
FDA Adverse Event
Injury
·MPRI·Product code LWS·October 6, 2016
STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·December 6, 2016