SEARCH RESULTS FOR: !➧주식DB구합니다◀✅텔레그램thinkDB(1545680 results)

Export results
Only the first 10,000 results were returned. Filter these results or refine your query. Some pre-built queries with more than 10,000 results are available for download.
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

Show Filters

The Arkis Precision Tunneler is designed to facilitate the subcutaneous passage of shunt tubing between two skin incisions when implanting a ventricular shunting system in patients with normal skin.
ARKIS BIOSCIENCES INC.
41.020.503
Not in Commercial Distribution

  • 00866614000177 ()
41.020.503

  • Subcutaneous tunneller, single-use
The Arkis Precision Tunneler is designed to facilitate the subcutaneous passage of shunt tubing between two skin incisions when implanting a ventricular shunting system in patients with normal skin.
ARKIS BIOSCIENCES INC.
41.020.502
Not in Commercial Distribution

  • 00866614000160 ()
41.020.502

  • Subcutaneous tunneller, single-use
The Arkis Precision Tunneler is designed to facilitate the subcutaneous passage of shunt tubing between two skin incisions when implanting a ventricular shunting system in patients with normal skin.
ARKIS BIOSCIENCES INC.
41.020.501
Not in Commercial Distribution

  • 00866614000153 ()
41.020.501

  • Subcutaneous tunneller, single-use
The Single Pass Tunneling Guidewire kit is designed to facilitate the subcutaneous passage of shunt tubing from a frontal scalp incision, or an incision on the neck, to an incision site on the torso when implanting a ventricular shunting system in patients greater than five (5) years old with a normal skull and normal skin.
ARKIS BIOSCIENCES INC.
41.157.101
Not in Commercial Distribution

  • 00866614000146 ()
41.157.101

  • Subcutaneous tunneller, single-use
The Single Pass Tunneling Guidewire kit is designed to facilitate the subcutaneous passage of shunt tubing from a frontal scalp incision, or an incision on the neck, to an incision site on the torso when implanting a ventricular shunting system in patients greater than five (5) years old with a normal skull and normal skin.
ARKIS BIOSCIENCES INC.
41.157.102
Not in Commercial Distribution

  • 00866614000139 ()
41.157.102

  • Subcutaneous tunneller, single-use
The Single Pass Tunneling Guidewire kit is designed to facilitate the subcutaneous passage of shunt tubing from a frontal scalp incision, or an incision on the neck, to an incision site on the torso when implanting a ventricular shunting system in patients greater than five (5) years old with a normal skull and normal skin.
ARKIS BIOSCIENCES INC.
41.157.103
Not in Commercial Distribution

  • 00866614000122 ()
41.157.103

  • Subcutaneous tunneller, single-use
The CerebroFlo EVD Catheter is a polyurethane catheter for diverting cerebrospinal fluid (CSF) from the ventricles of the brain through the drainage holes near the catheter's tip. The catheter is barium-sulfate impregnated to provide radiopacity. The CerebroFlo EVD Catheter is provided with a Stylette, Trocar, Barbed Leur Connector, Male Leur Cap, and a suture clip.
ARKIS BIOSCIENCES INC.
37.550.101
Not in Commercial Distribution

  • 00866614000108 ()

  • Outer Diameter: 3.3 Millimeter
  • Length: 35 Centimeter
37.550.101

  • Intracerebral infusion/drainage catheter, short-term
No Description
SARANAS INC.
FG001-02
In Commercial Distribution

  • 00866532000419 ()

  • 8 French


  • Femoral artery/vein access catheter
No Description
SARANAS INC.
FG001-01
In Commercial Distribution

  • 00866532000402 ()

  • 6 French


  • Femoral artery/vein access catheter
Outflow Sheath
Cannuflow, Inc.
ST-6-130
In Commercial Distribution

  • 20866497000374 ()
  • 00866497000370 ()

  • Outer Diameter: 5.8 Millimeter
  • Length: 130 Millimeter
TVST-6-130

  • Surgical irrigation/aspiration cannula, non-illuminating, single-use
< 1 ... 732 733 734 735 736 ... 1000 >