24 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MILLENNIUM 5000 MEUROVASCULAR COIL
FDA 510(k)
FDA Class 2
·Radiology
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·10304040091620·FILE - Channels RF File - Size 25.06 25MM
Multi-Link™
FDA UDI
AirLife Finland Oy·10190752179240·ECG Care Cable, 3 Lead with Integrated Grabber ...
Multi-Link
FDA UDI
Carefusion Finland 320 Oy·10885403256646·ECG Care Cable, 3 Lead with Integrated Grabber ...
Multi-Link™
FDA UDI
AirLife Finland Oy·10889483576205·Multi-Link™ ECG Care Cable, 3-ld w/ integrated ...
Multi-Link™
FDA UDI
AirLife Finland Oy·10190752179233·ECG Care Cable, 3 Lead with Integrated Grabber ...
Multi-Link™
FDA UDI
AirLife Finland Oy·10889483576199·Multi-Link™ ECG Care Cable, 3 Lead with integra...
OneTouch SureSoft
FDA UDI
LifeScan Europe GmbH·00353885006842·One Touch SureSoft Single Use Disposable Lancin...
ULTRAPOWER
FDA UDI
Conmed Corporation·10845854003459·ULTRAPOWER BUR, WIRE PASS (COPPER), 1.5MM
SHIMADZU WHOLE BODY X-RAY COMPUTED TOMOGRAPHY SCANNER SCT-7800TC
FDA 510(k)
FDA Class 2
·Radiology
POWDER FREE STERILE LATEX EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
ULTRAPOWER
FDA UDI
Conmed Corporation·10845854001745·ULTRAPOWER DEPTH LIMITING DRILL (COPPER), 1.1 X...
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR CLONMEL·Product code NIQ·August 5, 2010
ACCU-CHEK ® COMPACT TEST DRUM
FDA Adverse Event
Injury
·ROCHE DIAGNOSTICS·Product code LFR·March 26, 2013
CONCERTO CRT-D DR
FDA Adverse Event
Death
·MEDTRONIC MED REL, INC.·Product code NIK·March 16, 2011
ICY HOT HEAT THERAPY PATCH
FDA Adverse Event
Other
·CHATTEM, INC.·Product code IMD·March 27, 2008
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·October 20, 2021
PERCLOSE PROGLIDE¿
FDA Adverse Event
Injury
·ABBOTT VASCULAR INC.·Product code MGB·June 7, 2024
PDS CORD UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code NEW·August 12, 2021
XIENCE SKYPOINT DRUG ELUTING CORONARY STENT DELIVERY SYSTEM
FDA Adverse Event
Death
·ABBOTT VASCULAR·Product code NIQ·March 18, 2023