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

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FLIXENE IFG VASCULAR GRAFT

FDA 510(k)
FDA Class 2 ·Cardiovascular

CONMED

FDA UDI
Conmed Corporation·20653405002106·ELECTROSURGICAL FOOTSWITCH COVER

CONMED

FDA UDI
Conmed Corporation·30653405002103·ELECTROSURGICAL FOOTSWITCH COVER

ArgenZ ST 98x12 ML B4B

FDA UDI
ARGEN CORPORATION, THE·D818130142·Dental porcelain/ceramic restoration kit

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450189177·

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450267066·

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197043700·Ewald Hudson Tissue Forceps 12.0cm...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197540070·Caspar Rongeur straigth 2x12mm 140mm

AEQUALIS REVERSED SHOULDER PROSTHESIS

FDA 510(k)
FDA Class 2 ·Orthopedic

THERMACOOL TC SYSTEM

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

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·December 18, 2023

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·April 19, 2023

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

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

T:SLIM G5 SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code OYC·February 2, 2018

T:SLIM X2 INSULIN PUMP WITH INTEROPERABLE TECHNOLOGY (WITH T:CONNECT MOBILE APP)

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·November 26, 2024

HEMOCHRON SIGNATURE MICROCOAGULATION SYSTEM

FDA Adverse Event
Malfunction ·INTERNATIONAL TECHNIDYNE CORP.·Product code JPA·April 16, 2010

LEWIN BONE HOLD CLAMP 7

FDA Adverse Event
Malfunction ·INTEGRA YORK, PA INC·Product code LXH·May 21, 2013

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·September 30, 2014

SPRINT QUATTRO SECURE

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·June 16, 2011

ACTIVA

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·April 11, 2018