10,000 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DUODOPA_DUOPA
FDA Adverse Event
Injury
·ABBVIE MEDICAL DEVICE CENTER·Product code KNT·December 20, 2024
UNKNOWN KNEE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code NRA·October 9, 2017
VERITAS COLLAGEN MATRIX
FDA Adverse Event
Injury
·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·June 8, 2011
MCKESSON CONSULT U120
FDA Adverse Event
Injury
·ACON LABORATORIES, INC.·Product code JRE·February 1, 2019
CHEMSTRIP 10 UA
FDA Adverse Event
Death
·ROCHE DIAGNOSTICS·Product code JRE·May 6, 2002
MCKESSON CONSULT 120 URINE ANALYZER
FDA Adverse Event
Malfunction
·ACON LABORATORIES, INC.·Product code JRE·September 10, 2019
DUODOPA_DUOPA
FDA Adverse Event
Injury
·ABBVIE - MEDICAL DEVICE CENTER·Product code KNT·August 27, 2020
CARELINK PRO ONLINE
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code PHV·December 20, 2023
DUODOPA_DUOPA
FDA Adverse Event
Injury
·ABBVIE - MEDICAL DEVICE CENTER·Product code KNT·January 12, 2021
ENDEAVOR RX
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIQ·October 2, 2024
Refractometer For Clinical Use
FDA classification
FDA Class 1
·Refractometer For Clinical Use
DRE Med
FDA registration
DRE Med·50 products·🇺🇸 United States
CRE-MED
FDA registration
CRE-MED·1 product·🇺🇸 United States
Ares Trading SA
FDA registration
Ares Trading SA·1 product·🇨🇭 Switzerland
WE ARE RILEY LTD
FDA registration
WE ARE RILEY LTD·2 products·🇮🇪 Ireland
WE ARE DREAMERS LLC
FDA registration
WE ARE DREAMERS LLC·2 products·🇺🇸 United States
CRE BUFFER CRE DYE
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Duckworth & Kent
FDA UDI
DUCKWORTH AND KENT LIMITED·05055313831884·Capsulorhexis Forceps
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613119294·Calladine-Inamura Capsulorhexis Forceps, Ergono...
Duckworth & Kent
FDA UDI
DUCKWORTH AND KENT LIMITED·05055313831921·Capsulorhexis Forceps