17 results · 20ms · Sources: EU EUDAMED, US FDA

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TRIGLYCERIDE (TRINDER) PROCEDURE

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

Medline Industries, Inc.

FDA UDI
MEDLINE INDUSTRIES, INC.·10889942122387·PACK BIOPSY HCC11

JOBST Maternity

FDA UDI
BSN MEDICAL, INC.·04042809641394·OPAQUE MATERNITY 20-30 MM HG KNEE HIGH ZIG ZAG ...

Lucid Q-PTP / HWA 55

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

LUNDERQUIST WIRE GUIDE; DC WIRE GUIDE

FDA 510(k)
FDA Class 2 ·Cardiovascular

SPECTRUM INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·January 13, 2014

TENSION FREE VAGINAL TAPE

FDA Adverse Event
Injury ·ETHICON INC·Product code OTN·December 7, 2012

BRAVO PH CAPSULE DELIVERY DEVICE

FDA Adverse Event
Malfunction ·GIVEN IMAGING LTD.·Product code FFT·June 19, 2015

LUNDERQUIST EXTRA-STIFF DOUBLE CURVED EXCHANGE SUPPORT WIRE GUIDE

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DQX·February 16, 2017

LUNDERQUIST EXTRA-STIFF STRAIGHT EXCHANGE SUPPORT WIRE GUIDE

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DQX·July 10, 2017

LUNDERQUIST EXTRA-STIFF CURVED EXCHANGE SUPPORT WIRE GUIDE

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DQX·December 4, 2017

LUNDERQUIST EXTRA-STIFF DOUBLE CURVED EXCHANGE SUPPORT WIRE GUIDE

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DQX·February 9, 2017

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DQX·December 19, 2018

LUNDERQUIST EXTRA-STIFF CURVED EXCHANGE SUPPORT WIRE GUIDE

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DQX·April 20, 2017

LUNDERQUIST EXTRA-STIFF DOUBLE CURVED EXCHANGE SUPPORT WIRE GUIDE

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DQX·June 16, 2017

LUNDERQUIST SUPPORT WIRE GUIDE

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DQX·May 31, 2017

OEC 6800 Miniview, Image-intensified fluoroscopic x-ray system used during diagnostic, surgical and interventional procedures. Designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical orthopedic and extremity imagine. The device is not intended for whole-body pediatric imaging.

FDA Enforcement
Class I ·Terminated·GE OEC Medical Systems, Inc·August 1, 2012