10,000 results · 159ms · Sources: EU EUDAMED, US FDA

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Amvex Vacuum Regulator

FDA UDI
OHIO MEDICAL, LLC·00628101501501·VR-PP series, VacReg, Ped Int 2Mode 160mmHg, A...

AMD-RITMED

FDA UDI
AMD Medicom Inc·20686864051002·AMD-RITMED COHESIVE BANDAGE ROLL 4 Inch X 5 Yard

AMD-RITMED

FDA UDI
AMD Medicom Inc·20686864050418·AMD-RITMED COHESIVE BANDAGE ROLL 2 Inch X 5 Yard

CellaVision DC-1 PPA

FDA UDI
Cellavision AB·07350040975107·

PPA/BT-RB STETHOSCOPE

FDA 510(k)
FDA Class 2 ·Cardiovascular

PUPIL PATHWAY ANALYZER (PPA)

FDA 510(k)
FDA Class 1 ·Ophthalmic

ICU

FDA UDI
PRYOR PRODUCTS·00761887002722·6 LEG, SW, PA, 6 OUTLET, 6 HOOK RAKE, ASSEMBLED

RNK Products

FDA UDI
RNK PRODUCTS, INC.·00677986001019·PPA/BT-RB Module

CellaVision DC-1, CellaVision DC-1 PPA

FDA 510(k)
FDA Class 2 ·Hematology

prolaio Personalized Physiology Analytics Engine Software (PPA)

FDA UDI
Prolaio, Inc.·00850071330038·prolaio Personalized Physiology Analytics Engin...

ICU

FDA UDI
PRYOR PRODUCTS·00761887004719·Dual IV Stand Support Wheel w Tray Assembled

V-18 CONTROL WIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DQX·November 21, 2019

ELUVIA DRUG-ELUTING VASCULAR STENT SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIU·June 2, 2020

COMPLETE SE STENT SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC CARDIOVASCULAR·Product code NIO·May 26, 2010

ASPARTATE AMINOTRANSFERASE ACC. TO IFCC WITHOUT PYRIDOXAL PHOSPHATE ACTIVATION

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code CIT·June 16, 2015

AMS INFLATABLE PENILE PROSTHESIS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FHW·September 2, 2019

AMS INFLATABLE PENILE PROSTHESIS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FHW·April 1, 2020

AMS 800 URINARY CONTROL SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code EZY·March 17, 2020

ELUVIA DRUG-ELUTING VASCULAR STENT SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIU·August 19, 2020

SARS-COV-2 IGM

FDA Adverse Event
Malfunction ·ABBOTT IRELAND·Product code QKO·October 29, 2020