10,000 results
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51ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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IDL-LYSING REAGENT
FDA 510(k)
FDA Class 1
·Hematology
INDIGO MEDICAL MODEL IDL 830E
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
INDIGO MEDICAL MODEL IDL 830 & MODEL IDL 830E LASER SYSTEMS FOR GENERAL GYNECOLOGICAL APPLICATIONS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SET ZZ BASE ID-LE-WSM 3.0
FDA UDI
ZIRKONZAHN SRL·D800ZBCD5731·SET ZZ BASE ID-LE-WSM 3.0 (White Scanmarker and...
SET ZZ BASE ID-LE-WSM 3.5
FDA UDI
ZIRKONZAHN SRL·D800ZBCD5732·SET ZZ BASE ID-LE-WSM 3.5 (White Scanmarker and...
SET ZZ BASE ID-LE-WSM 5.7
FDA UDI
ZIRKONZAHN SRL·D800ZBCD5734·SET ZZ BASE ID-LE-WSM 5.7 (White Scanmarker and...
SET ZZ BASE ID-LE-WSM 4.5
FDA UDI
ZIRKONZAHN SRL·D800ZBCD5733·SET ZZ BASE ID-LE-WSM 4.5 (White Scanmarker and...
SPECTRA IDL SET
FDA Adverse Event
Malfunction
·TERUMO BCT INC.·Product code LKN·September 29, 2020
SPECTRA OPTIA IDL SET
FDA Adverse Event
Malfunction
·TERUMO BCT, INC.·Product code GKT·August 13, 2024
SPECTRA OPTIA IDL SET
FDA Adverse Event
Malfunction
·TERUMO BCT, INC.·Product code GKT·February 12, 2026
SPECTRA OPTIA IDL SET
FDA Adverse Event
Malfunction
·TERUMO BCT, INC.·Product code LKN·March 13, 2018
INDIGO PORTABLE LASER SYSTEM WITH TEMPERATURE FEEDBACK -MODEL IDL 830 (POWER OPTIONS : 25, 20, 15 & 10 WATTS) INDIGO FIB
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
LEICA BIOSYSTEMS
FDA Adverse Event
Injury
·LEICA BIOSYSTEMS NUSSLOCH·Product code IDL·November 28, 2018
LEICA RM2155
FDA Adverse Event
Injury
·LEICA BIOSYSTEMS GMBH·Product code IDL·September 15, 2011
LEICA RM2125
FDA Adverse Event
Malfunction
·LEICA BIOSYSTEMS, GMBH.·Product code IDL·September 30, 2011
LEICA RM2155
FDA Adverse Event
Injury
·LEICA BIOSYSTEMS, GMBH·Product code IDL·September 29, 2011
MICROM
FDA Adverse Event
Injury
·MICROM INTERNATIONAL GMBH·Product code IDL·April 1, 2011
LEICA RM2255
FDA Adverse Event
Injury
·LEICA BIOSYSTEMS GMBH·Product code IDL·November 2, 2011
MICROM
FDA Adverse Event
Injury
·MICROM INTL. GMBH·Product code IDL·April 6, 2011
ACCU-EDGE MICROTOME BLAADE DISPENSER
FDA Adverse Event
Injury
·MILES DIAGNOSTICS·Product code IDL·May 2, 1994