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

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DIAZYME HOMOCYSTEINE POC TEST KIT

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

Sklar

FDA UDI
SKLAR CORPORATION·10649111451607·CATLIN AMPUTATION KNIFE 11 INCHES

BOSS Instruments

FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515016293·Halsey NH, 5 1/2"

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450613108·

Eclipse Mini

FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522130755·ECLIPSE MINI ECG SENSORS, DEFIB SAFE (BOX OF 10)

Eclipse Mini

FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522130304·ECLIPSE MINI ECG SENSORS (BOX OF 10)

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970379·

SENTRYSUITE PRODUCT LINE

FDA 510(k)
FDA Class 2 ·Anesthesiology

OLYMPUS CF TYPE Y0023-L, Y0023I

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

TOTAL FEMUR

FDA Adverse Event
Injury ·STANMORE IMPLANTS WORLDWIDE·Product code KRO·June 7, 2018

SPECTRA WAVEWRITER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 17, 2024

CUSTOM PROXIMAL FEMUR IMPLANT

FDA Adverse Event
Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 23, 2014

CUSTOMER PROXIMAL FEMUR REPLACEMENT IMPLANT

FDA Adverse Event
Injury ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 19, 2014

CUSTOM TOTAL FEMUR REPLACEMENT IMPLANT

FDA Adverse Event
Injury ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 24, 2014

CUSTOM PROXIMAL FEMUR REPLACEMENT IMPLANT

FDA Adverse Event
Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code JWH·January 8, 2015

CONFIRM

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC, CRMD·Product code MXC·January 13, 2014

POWERED WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE TAYLOR STREET·Product code ITI·May 20, 2013

TM SHELL WITH CLUSTER HOLES

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code LPH·June 9, 2011

CUSTOM DISTAL FEMORAL IMPLANT

FDA Adverse Event
Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 23, 2014

UNK- NON- STANMORE HIP REPLACEMENT IMPLANT

FDA Adverse Event
Malfunction ·UNKNOWN·Product code KRO·June 25, 2015