55 results · 24ms · Sources: EU EUDAMED, US FDA

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Disposable Circular Staple, Disposable Hemorrhoidal Stapler, Disposable Linear Stapler and Reloads, Disposable Linear Cutter Stapler and Reloads, Disposable Endoscopic Linear Cutter Stapler and Reloads

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

Dornier Thulio Performance Fiber

FDA UDI
INNOVAQUARTZ LLC·00816959021887·

Dornier MedTech

FDA UDI
DORNIER MEDTECH AMERICA, INC.·00810116023448·THULIO LL-R TM 200µM 3M PERF. FIBER 3ST 10X USE

NA

FDA UDI
Synthes GmbH·10886982142177·2.4MM CORTEX SCREW SELF-TAPPING 9MM

Universal CE electrode-patch

FDA UDI
BRAEMAR MANUFACTURING, LLC·B146PE2C0·

ABSORBENT PAPER POINTS

FDA UDI
DiaDent Group International·08806383512732·"An absorbent paper points is an endodontic pap...

LAP-iX

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

CG-6108 ACT-IL CONTINUOUS ECG MONITOR AND ARRYTHMIA DETECTOR

FDA 510(k)
FDA Class 2 ·Cardiovascular

WALLSTENT ENDOPROSTHESIS WITH UNISTEP PLUS DELIVERY SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - GALWAY·Product code FGE·September 6, 2017

VALIANT STENT GRAFT

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code MIH·August 1, 2017

ATTAIN ABILITY

FDA Adverse Event
Injury ·MPRI·Product code OJX·June 8, 2017

VAPR HOOK ELECTRODE

FDA Adverse Event
Injury ·DEPUY MITEK·Product code GEI·October 27, 2014

ORTHOPAT PERIOPERATIVE AUTOTRANSFUSION SYSTEM

FDA Adverse Event
Malfunction ·HAEMONETICS CORP.·Product code CAC·August 4, 2011

SYNCHROMED II

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·July 2, 2013

ATTAIN ABILITY

FDA Adverse Event
Injury ·MPRI·Product code OJX·June 8, 2017

GORE VIABAHN® ENDOPROSTHESIS

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code NIP·October 26, 2016

GORE VIABAHN® ENDOPROSTHESIS

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code NIP·October 25, 2016

ATTAIN ABILITY PLUS

FDA Adverse Event
Injury ·MPRI·Product code OJX·June 8, 2017

SELECTSECURE

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code NVN·April 25, 2018

AMPLATZER® TORQVUE® (UNKNOWN)

FDA Adverse Event
Injury ·AGA MEDICAL CORPORATION·Product code DQY·April 23, 2020