35 results
·
20ms
·
Sources: EU EUDAMED, US FDA
OLYMPIC WARM-UP
FDA 510(k)
FDA Class 2
·Physical Medicine
ODYSSEY®
FDA UDI
Microport Orthopedics Inc.·M684KS0010561·
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00160561·
PowerPICC
FDA UDI
Bard Access Systems, Inc.·00801741225154·Catheter Placement Kit
artVeneer life
FDA UDI
Merz Dental GmbH·D7092001056·artVeneer life lower anteriors, UBXL, A2
AiroDyne M-set 36'' × 80'' QLT Burgundy Tridien
FDA UDI
Tridien Medical·00841965103951·AiroDyne M-set 36'' × 80'' QLT Burgundy Tridien
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·November 12, 2024
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·January 19, 2025
BIO-LIPID HUMAN SERUM HDL AND LDL CALIBRATORS
FDA 510(k)
FDA Class 1
·Clinical Chemistry
SMART SHIELD NON-STERILE POWDER-FREE PEPPERMINT SCENTED GREEN LATEX EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·October 28, 2024
9616240-2006-00341
FDA Adverse Event
Malfunction
·Product code FII·June 14, 2006
9616240-2006-00332
FDA Adverse Event
Other
·Product code FII·June 1, 2006
PHOENIX
FDA Adverse Event
Malfunction
·GAMBRO DASCO·Product code FII·May 10, 2006
9616240-2006-00339
FDA Adverse Event
Malfunction
·Product code FII·June 9, 2006
9616240-2006-00340
FDA Adverse Event
Malfunction
·Product code FII·June 9, 2006
9616240-2006-00350
FDA Adverse Event
Malfunction
·Product code FII·June 23, 2006
9616240-2006-00345
FDA Adverse Event
Malfunction
·Product code FII·June 14, 2006
CARDIOSAVE HYBRID, TYPE I PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·February 3, 2026
PHOENIX
FDA Adverse Event
Malfunction
·GAMBRO DASCO·Product code FII·May 10, 2006