SEARCH RESULTS FOR: 购买假的单位存款证明【咨询网:ｚｊｗ２１１.ｃｏｍ】宜城得克萨斯A(1853317 results)

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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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Valeo Spacer System - M555316000204

Tray 1, Phantom Plus PLIF, TLIF System Case 1
AMEDICA CORPORATION
A
Not in Commercial Distribution

  • M555316000204 ()
31-6000-204

  • Instrument tray, reusable

Valeo Spacer System - M555316000203

Tray 1, Phantom Plus PLIF, TLIF System Case 2
AMEDICA CORPORATION
A
Not in Commercial Distribution

  • M555316000203 ()
31-6000-203

  • Instrument tray, reusable

Phantom Plus Cage System - M555315200005

45° Double Sided Rasp
AMEDICA CORPORATION
A
Not in Commercial Distribution

  • M555315200005 ()
31-5200-005

  • Internal spinal fixation procedure kit, reusable

Phantom Plus Cage System - M555315200002

30° Left Fenestrated Cup Curette
AMEDICA CORPORATION
A
Not in Commercial Distribution

  • M555315200002 ()
31-5200-002

  • Internal spinal fixation procedure kit, reusable

Phantom Plus Cage System - M555315000003

Nerve_Root_Retractor_Sm_90_Dg
AMEDICA CORPORATION
A
Not in Commercial Distribution

  • M555315000003 ()
31-5000-003

  • Internal spinal fixation procedure kit, reusable

Phantom Plus Cage System - M555315000002

Nerve_Retractor_Bayonet
AMEDICA CORPORATION
A
Not in Commercial Distribution

  • M555315000002 ()
31-5000-002

  • Internal spinal fixation procedure kit, reusable

Phantom Plus Cage System - M555315000001

Nerve_Root_Retractor_Lg_90_Dg
AMEDICA CORPORATION
A
Not in Commercial Distribution

  • M555315000001 ()
31-5000-001

  • Internal spinal fixation procedure kit, reusable

Preference 2 - M555289000320

Complex Spine System Hook, Transverse Process, Right 5.5
AMEDICA CORPORATION
A
Not in Commercial Distribution

  • M555289000320 ()
28-9000-320

  • Bone-screw internal spinal fixation system hook

SafeBreak - Vascular - 10860635000311

SafeBreak Vascular is a Force-Activated Separation Device. It is intended to separate when excessive tension is exerted across a peripheral IV administration set. When SafeBreak Vascular separates, fluid flow is stopped from the infusion pump and blood flow is stopped from the patient’s IV catheter. SafeBreak Vascular is intended to aid in reduction of peripheral IV mechanical complications requiring IV replacement. SafeBreak Vascular is intended to be used on peripheral IV catheters in adults and adolescent populations eighteen (18) years of age and older receiving intermittent or continuous infusions with an electronic pump.
Lineus Medical
A
In Commercial Distribution

  • 10860635000311 ()
2855-01-0001

  • Luer/Luer breakaway connector

IVA Cage Ti - 08800039805650

Lateral Lumbar Interbody Fusion Titanium CageL45 x W18 x H9 x A6
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039805650 ()

  • Height: 9 Millimeter
TDI.45180609

  • Metallic spinal fusion cage, non-sterile
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