64 results
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56ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IRISpec
FDA UDI
IRIS INTERNATIONAL, INC.·10837461001973·IRISpec CA/CB Twinset
StatSpin
FDA UDI
IRIS INTERNATIONAL, INC.·10873037000766·CritSpin Digital Reader
iQ®200
FDA UDI
IRIS INTERNATIONAL, INC.·10837461002192·iQ® Lamina™ Cradle
iQ®200
FDA UDI
IRIS INTERNATIONAL, INC.·10837461002116·
vChem®
FDA UDI
IRIS INTERNATIONAL, INC.·10837461002536·vChem®10 SG Urine Chemistry Strips
iChem
FDA UDI
IRIS INTERNATIONAL, INC.·10837461002529·iChem®10 SG Urine Chemistry Strips
AX-4280
FDA UDI
IRIS INTERNATIONAL, INC.·10837461008002·AX-4280 Specific Gravity Calibrator Set
S4-IR-ETL
FDA Adverse Event
Injury
·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code LZS·June 14, 2019
ICHEMVELOCITY URINE CHEMISTRY SYSTEM
FDA Adverse Event
Malfunction
·IRIS INTERNATIONAL, INC.·Product code CDM·March 17, 2017
TECNIS OPTIBLUE ITEC PRELOADED 1-PIECE IOL
FDA Adverse Event
Malfunction
·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HQL·February 1, 2019
STAR
FDA Adverse Event
Injury
·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code LZS·February 1, 2019
STAR
FDA Adverse Event
Injury
·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code LZS·February 1, 2019
S4-IR-CE
FDA Adverse Event
Malfunction
·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code LZS·January 31, 2019
HEALON DUET PRO
FDA Adverse Event
Injury
·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code LZP·May 10, 2019
TECNIS OPTIBLUE ITEC PRELOADED 1-PIECE IOL
FDA Adverse Event
Injury
·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HQL·November 13, 2018
TECNIS
FDA Adverse Event
Injury
·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HQL·March 27, 2020
TECNIS OPTIBLUE 1-PIECE
FDA Adverse Event
Injury
·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HQL·August 16, 2019
STAR
FDA Adverse Event
Injury
·JOHNSON & JOHNSON SURGICAL VISION, INC·Product code LZS·July 11, 2018
CATALYS SYSTEM
FDA Adverse Event
Injury
·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code OOE·February 21, 2020
IRIS IQ 200 ELITE AUTOMATED URINE MICROSCOPY ANALYZER
FDA Adverse Event
Malfunction
·IRIS DIAGNOSITICS, A DIVISION OF IRIS INTERNATIONAL, INC.·Product code KQO·February 27, 2009