Medtronic Reusable Instruments

FDA UDI

MEDTRONIC SOFAMOR DANEK, INC.·00613994860392·CORONAL BENDER EX0810460 5.5 LEFT

NA

FDA UDI

Zimmer, Inc.·00889024060012·

Medtronic Reusable Instruments

FDA UDI

MEDTRONIC SOFAMOR DANEK, INC.·00613994860408·CORONAL BENDER EX0810461 5.5 RIGHT

Medtronic Reusable Instruments

FDA UDI

MEDTRONIC SOFAMOR DANEK, INC.·00613994853738·COMBO TOOL EX0810174 10 DEG REV BEND

n/a

FDA UDI

MEDTRONIC SOFAMOR DANEK, INC.·00643169273559·BENDER EX0812316 3.5MM ROD

NA

FDA UDI

Zimmer, Inc.·00889024034983·

Medtronic Reusable Instruments

FDA UDI

MEDTRONIC SOFAMOR DANEK, INC.·00613994860415·CORONAL BENDER EX0810462 6.35 LEFT

Compact

FDA UDI

VITALOGRAPH (IRELAND) LIMITED·05099169414846·GENERIC CLINICAL TRIAL CASE - MIP MEP COMPACT(1)

Medline

FDA UDI

MEDLINE INDUSTRIES, INC.·10884389958759·GUIDEWIRE, THREADED, 1.4 X 150MM

Medtronic Reusable Instruments

FDA UDI

MEDTRONIC SOFAMOR DANEK, INC.·00613994852632·BENDER EX0810457 STRAIGHT, RECTANGULAR

NA

FDA UDI

Zimmer, Inc.·00889024024311·

Medtronic Reusable Instruments

FDA UDI

MEDTRONIC SOFAMOR DANEK, INC.·00613994852717·BENDER EX0810456 6.35 IN-SITU RIGHT

Medtronic Reusable Instruments

FDA UDI

MEDTRONIC SOFAMOR DANEK, INC.·00643169047907·BENDER 5584255 5.5/6.0 IN-SITU LEFT

Medtronic Reusable Instruments

FDA UDI

MEDTRONIC SOFAMOR DANEK, INC.·00613994860422·CORONAL BENDER EX0810463 6.35 RIGHT

Instrument

FDA UDI

Jeil Medical Corporation·08809282811739·

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

FDA Pre-Market Approval

FDA Class 3 ·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room

System, Endovascular Graft, Aortic Aneurysm Treatment

FDA Pre-Market Approval

FDA Class 3 ·OVATION PRIME ABDOMINAL STENT GRAFT SYSTEM, OVATION IX ILIAC STENT GRAFT

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room

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

FDA Pre-Market Approval

FDA Class 3 ·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room