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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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STENT GRAFT VAMC3232B100TU VALCAP BARE
MEDTRONIC, INC.
VAMC3232B100TU
Not in Commercial Distribution

  • 00613994802767 ()

  • Stent Graft Covered Length 117 MM
  • Stent Graft Proximal Diameter 32 MM
  • Stent Graft Distal Diameter 32 MM


  • Descending thoracic aorta endovascular stent-graft
STENT GRAFT VAMC3434B100TU VALCAP BARE
MEDTRONIC, INC.
VAMC3434B100TU
Not in Commercial Distribution

  • 00613994802750 ()

  • Stent Graft Distal Diameter 34 MM
  • Stent Graft Proximal Diameter 34 MM
  • Stent Graft Covered Length 107 MM


  • Descending thoracic aorta endovascular stent-graft
STENT GRAFT VAMC3636B100TU VALCAP BARE
MEDTRONIC, INC.
VAMC3636B100TU
Not in Commercial Distribution

  • 00613994802743 ()

  • Stent Graft Distal Diameter 36 MM
  • Stent Graft Covered Length 107 MM
  • Stent Graft Proximal Diameter 36 MM


  • Descending thoracic aorta endovascular stent-graft
STENT GRAFT VAMC3838B100TU VALCAP BARE
MEDTRONIC, INC.
VAMC3838B100TU
Not in Commercial Distribution

  • 00613994802736 ()

  • Stent Graft Covered Length 107 MM
  • Stent Graft Distal Diameter 38 MM
  • Stent Graft Proximal Diameter 38 MM


  • Descending thoracic aorta endovascular stent-graft
STENT GRAFT VAMC4040B100TU VALCAP BARE
MEDTRONIC, INC.
VAMC4040B100TU
Not in Commercial Distribution

  • 00613994802729 ()

  • Stent Graft Covered Length 107 MM
  • Stent Graft Distal Diameter 40 MM
  • Stent Graft Proximal Diameter 40 MM


  • Descending thoracic aorta endovascular stent-graft
STENT GRAFT VAMC4242B100TU VALCAP BARE
MEDTRONIC, INC.
VAMC4242B100TU
Not in Commercial Distribution

  • 00613994802712 ()

  • Stent Graft Covered Length 112 MM
  • Stent Graft Proximal Diameter 42 MM
  • Stent Graft Distal Diameter 42 MM


  • Descending thoracic aorta endovascular stent-graft
The FLOSEAL Malleable Tip and Trimmable Tip are intended for delivery of FLOSEAL Hemostatic Matrix.
BAXTER HEALTHCARE CORPORATION
1502186
In Commercial Distribution

  • 50085412091001 ()
  • 00085412091006 ()
1502186

  • Collagen haemostatic agent, non-antimicrobial
Vysis Paraffin Pretreatment IV & Post-Hybridization Wash Buffer Kit
ABBOTT MOLECULAR INC.
01N31-005
In Commercial Distribution

  • 00884999000735 ()
01N31-005

  • Nucleic acid hybridization detection IVD, reagent
HYMOVIS® is based on an ultra-pure hyaluronan engineered using a proprietary process to increase viscosity, elasticity and residence time without chemical crosslinking.The hyaluronan in HYMOVIS® is derived from bacterial fermentation. HYMOVIS® is indicated for the treatment of pain in osteoarthritis (OA) of the knee in patients who have failed to respond adequately to conservative non-pharmacologic therapy or simple analgesics (e.g., acetaminophen). It is given by intra-articular injection in two injections given at weekly intervals.
FIDIA FARMACEUTICI SPA
FID185704
Not in Commercial Distribution

  • M71389122049663SAM1 ()
  • M71389122049663SAM0 ()

  • Total Volume: 3 Milliliter
FID185704

  • Synovial fluid supplementation medium
HYMOVIS® is based on an ultra-pure hyaluronan engineered using a proprietary process to increase viscosity, elasticity and residence time without chemical crosslinking.The hyaluronan in HYMOVIS® is derived from bacterial fermentation. HYMOVIS® is indicated for the treatment of pain in osteoarthritis (OA) of the knee in patients who have failed to respond adequately to conservative non-pharmacologic therapy or simple analgesics (e.g., acetaminophen). It is given by intra-articular injection in two injections given at weekly intervals.
FIDIA FARMACEUTICI SPA
89122-0496-63
Not in Commercial Distribution

  • M71389122049663A16 ()
  • M71389122049663 ()

  • Total Volume: 3 Milliliter
89122-0496-63

  • Synovial fluid supplementation medium
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