84 results
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38ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PEDERSON VAGINAL SPECULA
FDA 510(k)
FDA Class 1
·Obstetrics/Gynecology
DISPOSABLE PLASTIC VAGINAL SPECULA
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
DISPOSABLE PLASTIC VAGINAL SPECULA
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT
FDA 510(k)
FDA Class 1
·Obstetrics/Gynecology
VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT
FDA 510(k)
FDA Class 1
·Obstetrics/Gynecology
KLEENSPEC 590 PREMIUM VAG SPEC LG CASE
FDA Adverse Event
Malfunction
·WELCH ALLYN, INC·Product code HIB·June 29, 2017
KLEENSPEC 590 PREMIUM VAG SPEC LG CASE
FDA Adverse Event
Malfunction
·WELCH ALLYN·Product code HIB·June 29, 2017
ALLEGIANCE DISPOSABLE VAGINAL SPECULUM
FDA Adverse Event
Malfunction
·ALLEGIANCE/CARDINAL HEALTH·Product code HIB·October 24, 2008
KLEENSPEC 590 SERIES DISP. VAGINAL SPECULA
FDA Adverse Event
Malfunction
·WELCH ALLYN·Product code HIB·May 12, 2017
KLEENSPEC VAGINAL SPECULA
FDA Adverse Event
Malfunction
·WELCH ALLYN, INC.·Product code HIB·October 28, 2004
KLEENSPEC VAGINAL SPECULA
FDA Adverse Event
Other
·WELCH ALLYN, INC.·Product code HIB·June 2, 2004
KLEENSPEC VAGINAL SPECULA
FDA Adverse Event
Malfunction
·WELCH ALLYN, INC.·Product code HIB·October 28, 2004
KLEENSPEC VAGINAL SPECULA
FDA Adverse Event
Malfunction
·WELCH ALLYN, INC.·Product code HIB·October 28, 2004
DYNAREX VAGINAL SPECULA 4900, MODELS 4911-SMALL, 4912-MEDIUM, 4913-LARGE
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
KLEENSPEC VAGINAL SPECULA
FDA Adverse Event
Malfunction
·WELCH ALLYN, INC.·Product code HIB·October 28, 2004
KLEENSPEC VAGINAL SPECULA
FDA Adverse Event
Malfunction
·WELCH ALLYN, INC.·Product code HIB·October 28, 2004
KLEENSPEC VAGINAL SPECULA ILLUMINATION SYSTEM
FDA Adverse Event
Injury
·WELCH ALLYN, INC.·Product code HIB·January 14, 2010
GRAVES VAG SPECULUM MEDIUM 4 X 1-3/8IN
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code HDF·February 23, 2023
KLEENSPEC VAGINAL SPECULA ILLUMINATION
FDA Adverse Event
WELCH ALLYN·Product code HIB·June 25, 2012
KLEENSPEC 590 SERIES DISP. VAGINAL SPECULA
FDA Adverse Event
Malfunction
·WELCH ALLYN·Product code HIB·February 2, 2011