23 results · 29ms · Sources: EU EUDAMED, US FDA

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INTERFACE ARTERIAL BLOOD FILTER

FDA 510(k)
FDA Class 2 ·Cardiovascular

MP XRAYCER

FDA UDI
Innovative Orthopedic Technologies AG·03701602300259·MP XRAYCER

PURIST

FDA UDI
ADSM·03701091005536·MP XRAYCER

Bioplate®

FDA UDI
Bioplate, Inc.·M3848131310·Straight Plate - Ø1.5 mm - 2 hole - 14 mm

Bioplate®

FDA UDI
Bioplate, Inc.·M384813131CP1·Straight Plate - Ø1.5 mm - 2 hole - 14 mm

Bioplate®

FDA UDI
Bioplate, Inc.·M384813131US0·Straight Plate - Ø1.5 mm - 2 hole - 14 mm

BIOSCREW XTRALOK

FDA 510(k)
FDA Class 2 ·Orthopedic

LIASYS 450

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

LEG BAG WITH FLIP-FLO VALVE, NO STRAPS, 19 OZ., STERILE

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·August 28, 2020

LEG BAG WITH FLIP-FLO VALVE, NO STRAPS, 19 OZ., STERILE

FDA Adverse Event
Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code FAQ·August 14, 2024

LEG BAG WITH FLIP-FLO VALVE, NO STRAPS, 19 OZ., STERILE

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·December 13, 2020

LEG BAG WITH FLIP-FLO VALVE, NO STRAPS, 19 OZ., STERILE

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·March 4, 2020

LEG BAG WITH FLIP-FLO VALVE, NO STRAPS, 19 OZ., STERILE

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·May 14, 2018

LEG BAG WITH FLIP-FLO VALVE AND LATEX STRAPS, 32 OZ., STERILE

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·April 25, 2019

LEG BAG WITH FLIP-FLO VALVE AND LATEX STRAPS

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·April 29, 2019

V-PRO 1 PLUS STERILIZER

FDA Adverse Event
STERIS MEXICO, S. DE R.L. DE C.V.·Product code MLR·May 15, 2014

CARELINK PROGRAM W/TELEMETRY C

FDA Adverse Event
Malfunction ·MEDTRONIC, INC.·Product code DXY·October 31, 2012

INRATIO2

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·August 18, 2010

1018233-2018-05488

FDA Adverse Event
Malfunction ·November 16, 2018

LEG BAG WITH FLIP-FLO VALVE, NO STRAPS, 19 OZ., STERILE

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNX·September 14, 2022