DeVilbiss

FDA UDI

DEVILBISS HEALTHCARE LLC·00885304001140·IntelliPAP Standard Plus w/HH & SmartLink Modul...

GENESIS II

FDA UDI

Smith & Nephew, Inc.·00885556032411·GENESIS II SYMMETRICAL POSTERIOR ...

NA

FDA UDI

Synthes GmbH·10886982244093·2.0MM SCREW BLOCK F/SCREW MODULE SHELL F/MODULA...

IntelliVue CL Respiration Pod, SW Rev. B

FDA registration

Philips North America LLC·1 product·🇺🇸 United States

IntelliVue CL Respiration Pod, SW Rev. B

FDA registration

Philips North America LLC·1 product·🇺🇸 United States

IntelliVue CL Respiration Pod, SW Rev. B

FDA registration

Philips Electronics Ltd·1 product·🇨🇦 Canada

Lorracher Hip Abduct. Splint

FDA registration

Ottobock SE & Co. KGaA formerly known as Otto Bock Healthcare GmbH·1 product·🇩🇪 Germany

IntelliVue CL Respiration Pod, SW Rev. B

FDA registration

Philips Medizin Systeme Boeblingen GmbH·1 product·🇩🇪 Germany

Welch Allyn, Inc.

FDA UDI

WELCH ALLYN, INC.·00732094261349·ELI 380 upgrade to enable use with the WAM Wire...

Welch Allyn, Inc.

FDA UDI

WELCH ALLYN, INC.·00732094261356·ELI 380 upgrade to enable use with the WAM Wire...

Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

FDA Pre-Market Approval

FDA Class 3 ·Cardiac Resynchronization Therapy Defibrillator; Dynagen, Inogen, Origen, Autogen CRT-D's

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Implantable Cardioverter Defibrilllator/ Dynagen, Inogen, Origen and Autogen ICD's.

Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation

FDA Pre-Market Approval

FDA Class 3 ·FARAPULSE™ Pulsed Field Ablation System (FARAWAVE™ Pulsed Field Ablation Catheter, FARASTAR™ Catheter Connection Cable,

MAGIC LITE INTACT PTH DILUENT

FDA registration

Siemens Healthcare Diagnostics Inc.·1 product·🇺🇸 United States

MAGIC LITE INTACT PTH DILUENT

FDA registration

SIEMENS HEALTHCARE DIAGNOSTICS MANUFACTURING LTD·1 product·🇬🇧 United Kingdom

MAGIC LITE INTACT PTH DILUENT

FDA registration

SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED·1 product·🇬🇧 United Kingdom

MAGIC LITE INTACT PTH DILUENT

FDA registration

Siemens Healthcare Diagnostics Inc.·1 product·🇺🇸 United States

FDA Pre-Market Approval

BRAVA, BRAVA QUAD, VIVA QUAD, VIVA QUAD S, VIVA QUAD XT CRT-D, VIVA S CRT-D, VIVA XT CRT-D

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·EVERA S DR ICD, EVERA S VR ICD, EVERA XT DR ICD, EVERA XT VR ICD

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

FDA Pre-Market Approval

FDA Class 3 ·IntellaTip MiFi Filter Module, IntellaTip MiFi Reference Cable, EGM Cable, Maestro 4000 Footswitch