29 results · 28ms · Sources: EU EUDAMED, US FDA

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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