23 results
·
21ms
·
Sources: EU EUDAMED, US FDA
CARDIOZYME PLUS CK-MB ITEM #65045 (G)
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Arx
FDA UDI
Life Spine, Inc.·00190837131821·
Arx
FDA UDI
Life Spine, Inc.·00190837188948·
Arx
FDA UDI
Life Spine, Inc.·00190837131791·
Arx
FDA UDI
Life Spine, Inc.·00190837131814·
Arx
FDA UDI
Life Spine, Inc.·00190837190415·
Arx
FDA UDI
Life Spine, Inc.·00190837172879·
Arx
FDA UDI
Life Spine, Inc.·00190837175818·
Arx
FDA UDI
Life Spine, Inc.·00190837131807·
HEMASORB ABSORBABLE BONE HEMOSTAT MATRIX
FDA 510(k)
FDA Unclassified
·Unknown
22MM SITESELECT BREAST BIOPSY DEVICE MODEL SSD022
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
OMNIPOD 5 POD
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code QFG·June 1, 2023
OMNIPOD DASH INSULIN MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code LZG·October 3, 2023
OMNIPOD DASH INSULIN MANAGEMENT SYSTEM
FDA Adverse Event
Death
·INSULET CORPORATION·Product code LZG·July 19, 2023
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 15, 2014
CAPSUREFIX
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012
ECHELON*FLEX60
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 23, 2010
OMNIPOD DASH INSULIN MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code LZG·December 13, 2023
OMNIPOD DASH, PODS 10-PACK
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code LZG·May 9, 2023
OMNIPOD INSULIN MANAGEMENT SYSTEM
FDA Adverse Event
Injury
·INSULET CORPORATION·Product code LZG·January 23, 2024