25 results · 28ms · Sources: EU EUDAMED, US FDA

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eNAT molecular collection and preservation medium

FDA 510(k)
FDA Class 2 ·Microbiology

24M - Tampa Electric Co.

FDA UDI
Certified Safety Manufacturing, Inc.·00766588013497·24M Tampa Electric Co.

BICON DENTAL IMPLANT SYSTEM 3.0MM BICON DENTAL IMPLANT

FDA 510(k)
FDA Class 2 ·Dental

TAGG DISPOSABLE VAGINAL SPECULUM

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

Widex

FDA UDI
Widex A/S·05706069728194·Widex EVOKE E-FS (Tan silk S-440 ) Telecoil, RC...

ALLEVYN LIFE SACRUM (LARGE) PACK OF 10

FDA Adverse Event
Injury ·SMITH & NEPHEW MEDICAL LTD.·Product code KGX·October 25, 2019

ALLEVYN LIFE SACRUM (LARGE) PACK OF 10

FDA Adverse Event
Injury ·SMITH & NEPHEW MEDICAL LTD.·Product code KGX·October 25, 2019

ALLEVYN LIFE SACRUM (LARGE) PACK OF 10

FDA Adverse Event
Injury ·SMITH & NEPHEW MEDICAL LTD.·Product code KGX·October 25, 2019

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

CONTOUR TEST STRIPS (50)

FDA Adverse Event
Injury ·BAYER HEALTHCARE, LLC·Product code NBW·October 15, 2008

ENDEAVOR SPRINT RX CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code NIQ·August 5, 2011

BRONCHIAL THERMOPLASTY CATHETER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - SAN JOSE·Product code OOY·July 2, 2013

TRELLIS-6 PERIPHERAL INFUSION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC COVIDIEN·Product code KRA·June 7, 2018

TRELLIS-6 PERIPHERAL INFUSION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC COVIDIEN·Product code KRA·June 7, 2018

VENA SEAL CLOSURE SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code PJQ·February 12, 2020

PROTEGE GPS SELF-EXPANDING BILIARY STENT SYSTEM 018

FDA Adverse Event
Injury ·MEDTRONIC COVIDIEN·Product code FGE·June 7, 2018

PROTEGE GPS SELF-EXPANDING BILIARY STENT SYSTEM 018

FDA Adverse Event
Injury ·MEDTRONIC COVIDIEN·Product code FGE·June 7, 2018

PROTEGE GPS SELF-EXPANDING BILIARY STENT SYSTEM 018

FDA Adverse Event
Injury ·MEDTRONIC COVIDIEN·Product code FGE·June 7, 2018

BLAKE DRAIN UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GBX·January 5, 2022

HEARTMATE 3 LEFT VENTRICULAR ASSIST SYSTEM

FDA Adverse Event
Injury ·THORATEC CORPORATION·Product code DSQ·September 10, 2019