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

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VYGON STOPCOCKS & RAMPS(MANIFOLDS)

FDA 510(k)
FDA Class 2 ·Cardiovascular

Burr

FDA UDI
KATENA PRODUCTS, INC.·00841668120002·1mm Burr For Algerbrush II

Bioplate®

FDA UDI
Bioplate, Inc.·M3848131410·BioMesh® 3MC - 127 x 131 mm

Bioplate®

FDA UDI
Bioplate, Inc.·M384813141US0·BioMesh® 3MC - 127 x 131 mm

Bioplate®

FDA UDI
Bioplate, Inc.·M384813141CP0·BioMesh® 3MC - 127 x 131 mm

MICROGYN PLUS STIMULATION DEVICE

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

MICROLIFE DUAL MODE THERMOMETER,MODEL IFR1MJ1

FDA 510(k)
FDA Class 2 ·General Hospital

ACTIVA

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·May 15, 2014

CONSULTA CRT-D

FDA Adverse Event
Malfunction ·MEDTRONIC S.A.·Product code NIK·October 31, 2012

TRANSTAR STRETCHER

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FPO·August 18, 2010

Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

FDA Enforcement
Class II ·Terminated·STERILMED, INC.·December 16, 2015

Fortify, Sterile EO, Model #/ Part #: CD1231-40/100029238,100030095, 100041981; CD1231-40Q/100029229, 100030087, 100041982; CD1233-40/100029230, 100029250, 100029259,100031058, 100059778, 100070017; CD1233-40Q/100029260, 100029271, 100029277, 100031104, 100070089; CD1235-40/100029272, 100029282, 100029311, 100031039, 100059779; CD1235-40Q/100029273, 100029295, 100029312, 100030840; CD1241-40/100046351; CD1241-40Q/100046167; CD2231-40/100029274, 100030110, 100041922; CD2231-40Q/100029275, 100030089, 100041923; CD2233-40/100029147, 100029276, 100029313, 100031066, 100037043, 100048759, 100070007; CD2233-40Q/100029148, 100029263, 100029314, 100031067, 100037044, 100059770, 100070068; CD2235-40/100029149, 100029265, 100029283, 100031029, 100059837; CD2235-40Q/100029239, 100029258, 100029284, 100031030, 100066504; CD2241-40/100046148; CD2241-40Q/100046149; CD2299-40/100056952

FDA Enforcement
Class II ·Terminated·St Jude Medical Inc.·July 4, 2018