30 results · 32ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

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