30 results
·
36ms
·
Sources: EU EUDAMED, US FDA
AUTOMATED PHYSIOLOGIC PROFILE MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
Arx
FDA UDI
Life Spine, Inc.·00190837131678·
Arx
FDA UDI
Life Spine, Inc.·00190837188917·
Arx
FDA UDI
Life Spine, Inc.·00190837175788·
Arx
FDA UDI
Life Spine, Inc.·00190837131708·
Arx
FDA UDI
Life Spine, Inc.·00190837190385·
Arx
FDA UDI
Life Spine, Inc.·00190837172848·
Arx
FDA UDI
Life Spine, Inc.·00190837131692·
Arx
FDA UDI
Life Spine, Inc.·00190837131685·
TRUBYTE DENTURE BASE RESIN SYSTEM
FDA 510(k)
FDA Class 2
·Dental
WONDFO AMPHETAMINE URINE TEST, WONDFO BARBITURATES URINE TEST, WONDFO BENZODIAZEPINES URINE TEST
FDA 510(k)
FDA Class 2
·Clinical Toxicology
8.0MM/3.2MM DRILL SLEEVE 200MM
FDA Adverse Event
Malfunction
·SYNTHES HAGENDORF·Product code LXH·October 13, 2016
FISHER & PAYKEL HEALTHCARE
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code CAF·October 30, 2024
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 15, 2014
SIGMA 300 DR
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code DXY·October 31, 2012
ATTUNE CR FEM TRIAL SZ 6 LT
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS, INC.·Product code JWH·June 2, 2015
12.0MM/8.0MM PROTECTION SLEEVE 188MM
FDA Adverse Event
Malfunction
·SYNTHES HAGENDORF·Product code LXH·March 15, 2017
12.0MM/8.0MM PROTECTION SLEEVE 188MM
FDA Adverse Event
Malfunction
·SYNTHES HAGENDORF·Product code LXH·March 13, 2017
8.0MM/3.2MM DRILL SLEEVE 200MM
FDA Adverse Event
Malfunction
·SYNTHES HAGENDORF·Product code LXH·March 16, 2017
3.2MM THREE-FLUTED DRILL BIT QC/330MM/100MM CALIBRATION
FDA Adverse Event
Malfunction
·SYNTHES BETTLACH·Product code HTW·March 13, 2017