23 results · 38ms · Sources: EU EUDAMED, US FDA

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TF ROTARY NICKEL TITANIUM FILE

FDA 510(k)
FDA Class 1 ·Dental

STERILE LATEX EXAMINATION GLOVES (POWDERED) WITH PROTEIN CLAIM LESS THAN 100UG/G

FDA 510(k)
FDA Class 1 ·General Hospital

AT3C70 TRANSDUCER

FDA 510(k)
FDA Class 2 ·Radiology

CONTOUR THREAD OR CONTOUR THREADS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES (DBA ANGIOTECH)·Product code GAW·April 3, 2008

CONTOUR THREAD

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code GAW·February 15, 2008

EEA 28MM SINGLE-USE STAPLER

FDA Adverse Event
Injury ·COVIDIEN, FORMERLY USSC PUERTO RICO INC·Product code GDW·June 1, 2015

EEA31

FDA Adverse Event
Injury ·COVIDIEN, FORMERLY USSC PUERTO RICO INC·Product code GDW·August 31, 2015

CONTOUR THREAD OR CONTOUR THREADS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code GAW·February 12, 2013

CONTOUR THREAD OR CONTOUR THREADS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code GAP·September 16, 2008

CONTOUR THREAD OR CONTOUR THREADS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code GAW·September 23, 2009

CONTOUR THREAD OR CONTOUR THREADS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code GAW·May 15, 2008

CONTOUR THREAD OR CONTOUR THREADS

FDA Adverse Event
Injury ·SURGICAL SPECIALITIES CORP·Product code GAW·February 25, 2014

PREMIUM PLUS CEEA* 28 INSTR. W/TILT-TOP*

FDA Adverse Event
Injury ·COVIDIEN MEDICAL PRODUCTS (SHANGHAI) MAN·Product code GDW·November 4, 2015

COBAS E411 DISK SYSTEM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·April 17, 2013

OT PING METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 19, 2011

INTROCAN SAFETY

FDA Adverse Event
Other ·B. BRAUN MEDICAL, INC.·Product code FOZ·June 18, 2008

CONTOUR THREAD OR CONTOUR THREADS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP (DBA ANGIOTECH)·Product code GAW·October 22, 2009

DST SERIES ORVIL AUTOMATIC 25MM DEVICE

FDA Adverse Event
Injury ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GDW·April 25, 2016

CALCIUM

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES (IRVING IA/CC)·Product code CJY·September 1, 2020

EEA 31MM SINGLE-USE STAPLER

FDA Adverse Event
Injury ·COVIDIEN, FORMERLY USSC PUERTO RICO INC·Product code GAG·December 11, 2015