Permanent Pacemaker Electrode

FDA Pre-Market Approval

FDA Class 3 ·MEDTRONIC(R) CAPSURE(R) EPI PACING LEAD MODEL 4695

Permanent Pacemaker Electrode

FDA Pre-Market Approval

FDA Class 3 ·CAPSURE SP/SENSE/SP NOVUS

Tester, Pacemaker Electrode Function

FDA Pre-Market Approval

FDA Class 2 ·KENTROX RV 65, KENTROX RV 75, KAINOX SL 65/13, KAINOX SL 65/18

Permanent Pacemaker Electrode

FDA Pre-Market Approval

FDA Class 3 ·PHILOS PACING SYSTEM

Permanent Pacemaker Electrode

FDA Pre-Market Approval

FDA Class 3 ·PHILOS DR-T PULSE GENERATOR

Intimate Rose Rectal Dilator - Size 8

Basic UDI-DI

EU MDR · Eu Md Class 1 ·Plus EV Holdings·1 device

VERTEXA® Anorexie et Boulimie

Basic UDI-DI

EU MDR · Eu Md Class 1 ·VERTEXA·1 device

SPOTCHEM D CK

Basic UDI-DI

EU IVDD · Eu Ivd General ·ARKRAY Factory, Inc.·1 device

ACCELOGRAPH

FDA 510(k)

FDA Class 2 ·Anesthesiology

TOF-GUARD TRANSMISSION MONITOR

FDA 510(k)

FDA Class 2 ·Anesthesiology

AM 706 ELECTROMYOGRAPH, STIM., NEURO., EXTERNAL

FDA 510(k)

FDA Class 2 ·Physical Medicine

MINI ACCELOGRAPH NEUROMUSCULAR TRANS. MONITOR

FDA 510(k)

FDA Class 2 ·Anesthesiology

ACCELOGRAPH NEUROMUSCULAR TRANSMISSION MONITOR

FDA 510(k)

FDA Class 2 ·Anesthesiology

MYOTEST DBS NERVE STIMULATOR

FDA 510(k)

FDA Class 2 ·Anesthesiology

MYOGRAPH 2000 - NEURO. TRANS. MONITOR & RECORDING

FDA 510(k)

FDA Class 2 ·Anesthesiology

ELPHA 2000

FDA 510(k)

FDA Class 2 ·Physical Medicine

MYOTEST - NERVE STIMULATOR

FDA 510(k)

FDA Class 2 ·Anesthesiology

System, Endovascular Graft, Aortic Aneurysm Treatment

FDA Pre-Market Approval

FDA Class 3 ·Valiant Navion Thoracic Stent Graft System

BE24/00000082

Certificate

IVDD Annex III Section 6·D-tek s.a.·SGS United Kingdom Limited·17 Basic UDI-DIs

BE24-00000082

Certificate

IVDD Annex III Section 6·D-tek s.a.·SGS United Kingdom Limited·7 Basic UDI-DIs