SCHOOL TRAUMA ADVANCED RESPONSE KIT

FDA UDI

Safeguard US Operating, LLC·M689SHSTARTPAXSM010·(1) TMT (Tactical Mechanical Tourniquet) (1) Ce...

PATIENT EXAMINATION GLOVE (LATEX)

FDA 510(k)

FDA Class 1 ·General Hospital

NA

FDA UDI

MEDTRONIC, INC.·00763000358822·CUSTOM PACK HY10Y68R4 3/8HEARTASST

DORO® Lubricant HP500

FDA UDI

pro med instruments GmbH, Herstellung und Vertrieb medizinisch technischer Ausrüstung·04250435526996·DORO® Lubricant HP500

DORO® Lubricant HP500

FDA UDI

pro med instruments GmbH, Herstellung und Vertrieb medizinisch technischer Ausrüstung·04250435528129·DORO® Lubricant HP500, Six-pack

KLYO

FDA UDI

KLYO MEDICAL SYSTEMS INC.·B773KLTEM77·Mobile, electro- motorized table designed to be...

Stent, Superficial Femoral Artery, Drug-Eluting

FDA Pre-Market Approval

FDA Class 3 ·Zilver® PTX® Peripheral Drug- Eluting Stent

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·VENTAK PRX AND VENTAK. MINI AUTOMATIC IMPLANTABLE CARDIOVERTER

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·VENTAK(R) PRX (TM) MODEL 1700,1705 PULSE GENERATOR

Stent, Superficial Femoral Artery, Drug-Eluting

FDA Pre-Market Approval

FDA Class 3 ·Zilver® PTX® Drug-Eluting Peripheral Stent

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·VENTAK(R) PRX (TM) MODEL 1700,1705 PULSE GENERATOR

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·VENTAK PRX AND VENTAK MINI AUTOMATIC IMPLANTABLE CARDIOVERTER

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·VENTAK(R) PRX (TM) MODEL 1700,1705 PULSE GENERATOR

Stent, Superficial Femoral Artery, Drug-Eluting

FDA Pre-Market Approval

FDA Class 3 ·Zilver® PTX® Peripheral Drug-Eluting Stent

Stent, Superficial Femoral Artery, Drug-Eluting

FDA Pre-Market Approval

FDA Class 3 ·Zilver® PTX® Drug-Eluting Peripheral Stent

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Ventak(R) PRX (TM) Model 1700,1705 Pulse Generator

Stent, Superficial Femoral Artery, Drug-Eluting

FDA Pre-Market Approval

FDA Class 3 ·Zilver® PTX® Peripheral Drug-Eluting Stent

Stent, Superficial Femoral Artery, Drug-Eluting

FDA Pre-Market Approval

FDA Class 3 ·Zilver® PTX® Drug-Eluting Peripheral Stent

Lumbar IBFD

FDA UDI

KEOS·B084KPS12308160·

Lumbar IBFD

FDA UDI

KEOS·B084KPS12308070·