312 results · 31ms · Sources: EU EUDAMED, US FDA

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N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR89300051·Mand. 1. Molar band W-Fit right 05

CHIMAERA Hip Fracture System

FDA UDI
ORTHOFIX SRL·18054242514848·CHIMAERA HFS END CAP L5MM STERILE

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR89300050051·Mand. 1. Molar band W-Fit right 05

Breeze Nasal Airway

FDA UDI
Summit Medical, Inc.·00385640000147·

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR89300050101·Mand. 1. Molar band W-Fit right 05

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR89300050501·Mand. 1. Molar band W-Fit right 05

Guided Surgery

FDA UDI
BICON, LLC·00813110026149·3.0mm Guided Surgery Rings

Grasping forceps

FDA UDI
SOPRO-COMEG GmbH·04059082022772·

DRITRAINER

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

SAVINA 300

FDA Adverse Event
Malfunction ·DRAGER MEDICAL GMBH·Product code CBK·June 9, 2015

HARMONIC ACE PLUS 7 W ADV HEMOSTASIS

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·November 20, 2017

STERIS SYSTEM 1E

FDA Adverse Event
STERIS CORPORATION - HOPKINS·Product code MED·January 25, 2013

7900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·December 2, 2010

TELIGEN

FDA Adverse Event
Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 11, 2014

HARMONIC ACE

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·November 7, 2017

BD SERO-FUGE¿ 2001 CENTRIFUGE, 1 SPEED, 115V

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO.·Product code LXG·October 10, 2019

Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

FDA Pre-Market Approval
FDA Class 3 ·CONTAK RENEWAL MODELS H125 AND H120 WITH THE MODEL 2865 VERSION 1.8 APPLICATION SOFTWARE

Prosthesis, Breast, Noninflatable, Internal, Silicone Gel-Filled

FDA Pre-Market Approval
FDA Class 3 ·Motiva SmoothSilk Round Ergonomix Silicone Gel-Filled Breast Implants, Motiva SmoothSilk Round Silicone Gel-Filled Breas

Catheter, Coronary, Atherectomy

FDA Pre-Market Approval
FDA Class 3 ·DIAMONDBACK 360 CORONARY ORBITAL ATHERECTOMY SYSTEM

Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

FDA Pre-Market Approval
FDA Class 3 ·CONTAK RENEWAL TR FAMILY