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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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U/P Root Canal Powder - D6870011435FG0

U/P Root Canal Powder, Liquid (1/8 oz/3.5 ml)
DENTSPLY INTERNATIONAL INC.
0011435FG
Not in Commercial Distribution

  • D6870011435FG0 ()

  • Total Volume: 3.5 Milliliter
  • 1 Bottle Liquid (3.5 mL)
0011435FG

  • Hygroscopic dental cement

U/P Root Canal Powder - D6870011430FG0

U/P Root Canal Powder, Powder (1/2 oz/15 g)
DENTSPLY INTERNATIONAL INC.
0011430FG
Not in Commercial Distribution

  • D6870011430FG0 ()

  • 1 Bottle Powder (15 g)
  • Weight: 15 Gram
0011430FG

  • Hygroscopic dental cement

U/P Root Canal Powder - D6870011431FG1

U/P Root Canal Powder, Powder (2 oz/60 g)
DENTSPLY INTERNATIONAL INC.
0011431FG
Not in Commercial Distribution

  • D6870011431FG1 ()
  • D6870011431FG0 ()

  • 1 Bottle Powder (2 oz/60 g)
  • Weight: 60 Gram
0011431FG

  • Hygroscopic dental cement

LACRIFLOW - 04540778140875

The LACRIFLOW is indicated in treatments of epiphora in-patients 12 months and older, in cases of: - Canalicular pathologies (stenosis, obstruction, lacerations), - During Dacryocystorhinostomy (conventional or laser), - Congenital nasolacrimal duct obstruction.
KANEKA CORPORATION
LF-R090A
In Commercial Distribution

  • 04540778140875 ()
  • 14540778140872 ()

  • Length: 90 Millimeter


  • Lacrimal tube

LACRIFLOW - 04540778140868

The LACRIFLOW is indicated in treatments of epiphora in-patients 12 months and older, in cases of: - Canalicular pathologies (stenosis, obstruction, lacerations), - During Dacryocystorhinostomy (conventional or laser), - Congenital nasolacrimal duct obstruction.
KANEKA CORPORATION
LF-R105A
In Commercial Distribution

  • 04540778140868 ()
  • 14540778140865 ()

  • Length: 105 Millimeter


  • Lacrimal tube

LACRIFLOW CL - 04540778171398

The Lacriflow CL is indicated in treatments of epiphora in patients 12 months and older, in cases of: - Canalicular pathologies (stenosis, obstruction, lacerations), - During Dacryocystorhinostomy (conventional or laser), - Congenital nasolacrimal duct obstruction.
KANEKA CORPORATION
LF-CL090A
In Commercial Distribution

  • 14540778171395 ()
  • 04540778171398 ()

  • Length: 90 Millimeter


  • Lacrimal tube

LACRIFLOW CL - 04540778171381

The Lacriflow CL is indicated in treatments of epiphora in patients 12 months and older, in cases of: - Canalicular pathologies (stenosis, obstruction, lacerations), - During Dacryocystorhinostomy (conventional or laser), - Congenital nasolacrimal duct obstruction.
KANEKA CORPORATION
LF-CL105A
In Commercial Distribution

  • 04540778171381 ()
  • 14540778171388 ()

  • Length: 105 Millimeter


  • Lacrimal tube

Illico FS - 00844856068711

FACET LAG SCREW, 5.0mm X 40mm
ALPHATEC SPINE, INC.
74350-40
In Commercial Distribution

  • 00844856068711 ()

  • Length: 40 Millimeter
  • Outer Diameter: 5 Millimeter


  • Spinal bone screw, non-bioabsorbable

Illico FS - 00844856068704

FACET LAG SCREW, 5.0mm X 35mm
ALPHATEC SPINE, INC.
74350-35
In Commercial Distribution

  • 00844856068704 ()

  • Length: 35 Millimeter
  • Outer Diameter: 5 Millimeter


  • Spinal bone screw, non-bioabsorbable

Illico FS - 00844856068698

FACET LAG SCREW, 4.5mm X 45mm
ALPHATEC SPINE, INC.
74345-45
In Commercial Distribution

  • 00844856068698 ()

  • Length: 45 Millimeter
  • Outer Diameter: 4.5 Millimeter


  • Spinal bone screw, non-bioabsorbable
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