29 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
RESPONSE ELECTROPHYSIOLOGY CATHETER, SUPREME ELECTROPHYSIOLOGY CATHETER, MODEL 401XXX AND 401XXX
FDA 510(k)
FDA Class 2
·Cardiovascular
XLIF
FDA UDI
Nuvasive, Inc.·00195377160263·XLIF Prone Instrument Tray
STC BARBITURATES INTERCEPT MICRO-PLATE EIA, MODEL 1108I
FDA 510(k)
FDA Class 2
·Clinical Toxicology
DIAMOND (MAMMOGRAPHIC X-RAY SYSTEM)
FDA 510(k)
FDA Class 2
·Radiology
ULTRACISION HARMONIC SCALPEL HAND PIECE
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 13, 2006
ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54, 55
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code LFL·June 15, 2006
ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 19, 2006
ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code LFL·June 15, 2006
ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54, 55
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code LFL·June 15, 2006
ULTRACISION HARMONIC SCALPEL HAND PIECE
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006
ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006
ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54, 55
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code LFL·June 7, 2006
ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 19, 2006
ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006
ULTRACISION HARMONIC SCALPEL HAND PIECE
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 13, 2006
ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code LFL·June 16, 2006
PK DISSECTING FORCEPS INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·March 13, 2013
4 MOTOR ADVANCE BED
FDA Adverse Event
Malfunction
·HILL-ROM INC.·Product code FNL·February 8, 2011
IMMULITE 2500
FDA Adverse Event
Death
·SIEMENS MEDICAL SOLUTIONS DIAGNOSTICS·Product code JJQ·February 22, 2008
APTIMA SARS-COV-2 ASSAY
FDA Adverse Event
Malfunction
·HOLOGIC INCORPORATED·Product code QJR·July 27, 2022