30 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DISPOSABLE LAPAROSCOPIC ELECTRODE, DISPOSABLE LAPAROSCOPIC ELECTRODE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PENCIL,ABC,BEND-A-BEAM,6" LONG
FDA Adverse Event
Malfunction
·CONSOLIDATED MEDICAL EQUIPMENT COMPANY·Product code GEI·April 17, 2024
ABC® Bend-A-Beam®
FDA UDI
Conmed Corporation·10653405002758·ABC® Bend-A-Beam® Handpiece Handcontrol Malleab...
Bard® Polyurethane Ureteral Catheters, Open Tip
FDA UDI
C. R. Bard, Inc.·10801741126908·Bard® Polyurethane Ureteral Catheters, Open Tip
ABC® BEND-A-BEAM®
FDA Adverse Event
Injury
·CONMED·Product code GEI·February 18, 2026
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197304009·Verhoeven-Rosen Suction tube
Ø0,6mm...
BIODESIGN SURGISIS ANTERIOR POSTERIOR PELVIC FLOOR GRAFTS
FDA 510(k)
FDA Class 3
·Obstetrics/Gynecology
ILLUMINA MISEQDX CYSTIC FIBROSIS 139-VARIANT ASSAY
FDA 510(k)
FDA Class 2
·Immunology
NA
FDA UDI
STRYKER CORPORATION·04546540731647·6.0mm Caspar Blade
ABC BEND-A-BEAM
FDA Adverse Event
Malfunction
·CONSOLIDATED MEDICAL EQUIPMENT COMPANY·Product code GEI·August 5, 2024
PENCIL,ABC,BEND-A-BEAM,6" LONG
FDA Adverse Event
Malfunction
·CONSOLIDATED MEDICAL EQUIPMENT COMPANY·Product code GEI·April 29, 2024
6" BEND-A-BEAM MALABLE ABC HP
FDA Adverse Event
Malfunction
·CONSOLIDATED MEDICAL EQUIPMENT·Product code GEI·October 30, 2018
6" INCH BEND A BEAM MALABLE ABC HANDPIECE
FDA Adverse Event
Malfunction
·CONSOLIDATED MEDICAL EQUIPMENT·Product code GEI·November 13, 2018
ABC® BEND-A-BEAM®
FDA Adverse Event
Malfunction
·CONSOLIDATED MEDICAL EQUIPMENT COMPANY·Product code GEI·September 26, 2025
PENCIL,ABC,BEND-A-BEAM,6" LONG
FDA Adverse Event
Malfunction
·CONSOLIDATED MEDICAL EQUIPMENT COMPANY·Product code GEI·November 2, 2022
ABC® BEND-A-BEAM®
FDA Adverse Event
Malfunction
·CONSOLIDATED MEDICAL EQUIPMENT COMPANY·Product code GEI·January 28, 2025
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 2, 2014
AEQUALIS
FDA Adverse Event
Injury
·TORNIER SAS·Product code KWS·May 23, 2013
MAXIMO II DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code LWS·June 20, 2011
ABC Bend-A-Beam Handpiece REF 134006 Handcontrol Malleable Handpiece, 6" (15.2 cm) QTY: 1 STERILE CONMED CORPORATION 525 FRENCH RD UTICA, NY 13205 ASSEMBLED IN MEXICO (Pouch label) ABC Bend-A-Beam Handpiece REF 134006 Handcontrol Malleable Handpiece, 6" (15.2 cm) QTY: 10 STERILE CONMED CORPORATION 525 FRENCH RD UTICA, NY 13205 ASSEMBLED IN MEXICO (case label) Usage: Electrosurgical handpiece for use as monopolar electrosurgical accessory in conjunction with CONMED electrosurgical units equipped with argon beam coagulation.
FDA Recall
Terminated
·ConMed Electrosurgery·Product code GEI·December 18, 2008