22 results · 24ms · Sources: EU EUDAMED, US FDA

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AN1036 Dosimeter

FDA 510(k)
FDA Class 2 ·General Hospital

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772777662·LUMBAMED BASIC DORSAL STAYS M SILVER IV

StarDental Instrument Solutions

FDA UDI
DENTALEZ, INC.·D7022003340·CLASSIQUE DIA INSTRUMENTS 701-9P

Integra® Jarit®

FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780466727·Integra® Jarit® Sofield Retractor, Double-Ended...

PILLING

FDA UDI
TELEFLEX INCORPORATED·04026704417834·SPONGE TONSIL STERILE XRAY GAUZE LARGE 500/ BOX

METZENBAUM SCISSORS

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896054783·METZENBAUM SCISSORS DELICATE STRAIGHT BLADES PO...

IMPACT MODULAR TOTAL HIP SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

INSULATION AND CONTINUITY TESTER PLUS ACCESSORIES; MODELS ATI014 & ATI014 FC

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·July 28, 2025

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·February 1, 2022

ACTIVA

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·October 24, 2014

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 11, 2011

MECHANICAL (MANUAL) WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE TAYLOR STREET·Product code IOR·July 1, 2013

PLATE, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HRS·October 26, 2016

PLATE, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HRS·October 26, 2016

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·October 26, 2016

PLATE, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HRS·October 26, 2016

OT VERIO FLEX METER

FDA Adverse Event
Injury ·LIFESCAN EUROPE GMBH·Product code NBW·June 17, 2020

OT VERIO FLEX METER

FDA Adverse Event
Injury ·LIFESCAN EUROPE GMBH·Product code NBW·June 17, 2020

UNK - SCREWS: CANNULATED

FDA Adverse Event
Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·March 17, 2020