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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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No Description
Provision
VS101015P
Not in Commercial Distribution

  • B504VS101015P0 ()
  • B504VS101015P1 ()


  • Laparoscopic access cannula, reprocessed
No Description
Provision
VS101012P
In Commercial Distribution

  • B504VS101012P0 ()
  • B504VS101012P1 ()


  • Laparoscopic access cannula, reprocessed
No Description
Provision
VS101011P
Not in Commercial Distribution

  • B504VS101011P0 ()
  • B504VS101011P1 ()


  • Laparoscopic access cannula, reprocessed
No Description
Provision
VS101005
Not in Commercial Distribution

  • B504VS1010050 ()
  • B504VS1010051 ()


  • Laparoscopic access cannula, reprocessed
No Description
Provision
UNVCA5STF
Not in Commercial Distribution

  • B504UNVCA5STF0 ()
  • B504UNVCA5STF1 ()


  • Laparoscopic access cannula, reprocessed
No Description
Provision
UNVCA5LGF
Not in Commercial Distribution

  • B504UNVCA5LGF0 ()
  • B504UNVCA5LGF1 ()


  • Laparoscopic access cannula, reprocessed
No Description
Provision
UNVCA12STS
Not in Commercial Distribution

  • B504UNVCA12STS0 ()
  • B504UNVCA12STS1 ()


  • Laparoscopic access cannula, reprocessed
No Description
Provision
UNVCA12STF
Not in Commercial Distribution

  • B504UNVCA12STF0 ()
  • B504UNVCA12STF1 ()


  • Laparoscopic access cannula, reprocessed
No Description
Provision
UNVCA12LGF
Not in Commercial Distribution

  • B504UNVCA12LGF0 ()
  • B405UNVCA12LGF1 ()


  • Laparoscopic access cannula, reprocessed
Cytoflex® Tef-Guard® is a non-resorbable membrane for use as a space-making barrier in guided tissue regeneration procedures. Composed of a proprietary micro-porous polytetrafluoroethylene (ePTFE) thin film, Cytoflex® Tef-Guard® has a surface texture and porosity suitable for adhesion of host cells to the material while blocking passage and integration of bacteria within the interstices of the material. The supple membrane conforms easily to tissue contours, and yet offers sufficient stiffness to maintain a space over the bony defect. The micro porous surface is designed to improve flap attachment but prevent tissue and bacteria ingrowth. Cytoflex® Tef-Guard® is for use as a barrier membrane for guided tissue regeneration procedures. Composed of a proprietary micro-porous polytetrafluoroethylene (ePTFE), the textured version of Cytoflex® Tef-Guard® has superficial macro texture overlapping the micro pore texture on both surfaces. The cellular level micro texture is invisible to the naked eye, but can be seen at high magnifications. The macro texture provides additional grips for flap attachment.
UNICARE BIOMEDICAL INC.
TEX-200
In Commercial Distribution

  • D767C0402010 ()
  • D767C0402051 ()
C04-0201

  • Pliable-polymer dental regeneration membrane, non-bioabsorbable
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