SEARCH RESULTS FOR: ("Make Dominican School of Philosophy")(70001 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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Zilver Vena - 10827002574356

Zilver Vena, Venous Self-Expanding Stent
COOK IRELAND LTD
G57435
In Commercial Distribution

  • 10827002574356 ()
ZVT7-35-80-12-140

  • Bare-metal peripheral venous stent

Zilver Vena - 10827002574349

Zilver Vena, Venous Self-Expanding Stent
COOK IRELAND LTD
G57434
In Commercial Distribution

  • 10827002574349 ()
ZVT7-35-80-12-100

  • Bare-metal peripheral venous stent

Zilver Vena - 10827002574332

Zilver Vena, Venous Self-Expanding Stent
COOK IRELAND LTD
G57433
In Commercial Distribution

  • 10827002574332 ()
ZVT7-35-80-12-60

  • Bare-metal peripheral venous stent

Zilver Vena - 10827002574325

Zilver Vena, Venous Self-Expanding Stent
COOK IRELAND LTD
G57432
In Commercial Distribution

  • 10827002574325 ()
ZVT7-35-80-12-40

  • Bare-metal peripheral venous stent

Zilver Vena - 10827002574318

Zilver Vena, Venous Self-Expanding Stent
COOK IRELAND LTD
G57431
In Commercial Distribution

  • 10827002574318 ()
ZVT7-35-80-10-140

  • Bare-metal peripheral venous stent

Zilver Vena - 10827002574301

Zilver Vena, Venous Self-Expanding Stent
COOK IRELAND LTD
G57430
In Commercial Distribution

  • 10827002574301 ()
ZVT7-35-80-10-100

  • Bare-metal peripheral venous stent

Zilver Vena - 10827002574295

Zilver Vena, Venous Self-Expanding Stent
COOK IRELAND LTD
G57429
In Commercial Distribution

  • 10827002574295 ()
ZVT7-35-80-10-60

  • Bare-metal peripheral venous stent

Zilver Vena - 10827002574288

Zilver Vena, Venous Self-Expanding Stent
COOK IRELAND LTD
G57428
In Commercial Distribution

  • 10827002574288 ()
ZVT7-35-80-10-40

  • Bare-metal peripheral venous stent

Dermagraft - 00618474000015

Dermagraft is indicated for use in the treatment of full-thickness diabetic foot ulcers greater than six weeks duration, which extend through the dermis, but without tendon, muscle, joint capsule, or bone exposure. Dermagraft should be used in conjunction with standard wound care regimens and in patients that have adequate blood supply to the involved foot.
ORGANOGENESIS INC.
1
In Commercial Distribution

  • 00618474000015 ()


  • Skin regeneration template, human-/animal-derived

PRISMAFLEX TPE 2000 SET - 07332414111038

The Prismaflex TPE2000 set is indicated for use only with the PrismaFlex control unit or with the PrisMax control unit (in countries where PrisMax is cleared or registered), after having selected TPE therapy. The Prismaflex TPE2000 set is intended for use in therapeutic plasma exchange, thus in diseases where removal of plasma components in indicated.
GAMBRO INDUSTRIES
114093
In Commercial Distribution

  • 07332414111038 ()
  • 37332414111039 ()
114093

  • Apheresis system filter, whole blood
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