SEARCH RESULTS FOR: 得克萨斯A(72209 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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No Description
ACRE PHARMA LIMITED
N/A
In Commercial Distribution

  • 05060604130072 ()


  • Dermal tissue reconstructive material, animal-derived
No Description
ACRE PHARMA LIMITED
N/A
In Commercial Distribution

  • 05060604130065 ()


  • Synovial fluid supplementation medium
No Description
ACRE PHARMA LIMITED
N/A
In Commercial Distribution

  • 05060604130041 ()
  • 05060604130058 ()


  • Synovial fluid supplementation medium
No Description
PAVAN TRADING LTD
N/A
In Commercial Distribution

  • 05060548950071 ()


  • Synovial fluid supplementation medium
Rigid Gas Permeable Contact Lens
Bausch & Lomb Incorporated
oprifocon A
In Commercial Distribution

  • 00785811435639 ()
Boston Equalens II

  • Rigid-gas-permeable corrective contact lens, extended-wear
  • Orthokeratology contact lens
Rigid Gas Permeable Contact Lens
Bausch & Lomb Incorporated
itaflurofocon A
In Commercial Distribution

  • 00785811435622 ()
Boston Equalens

  • Rigid-gas-permeable corrective contact lens, extended-wear
Superion Dilator 1
VERTIFLEX, INC.
N/A
Not in Commercial Distribution

  • 00884662000369 ()
100-9146

  • Lumbar interspinous decompression instrument set, reusable
Superion Handle
VERTIFLEX, INC.
N/A
Not in Commercial Distribution

  • 00884662000352 ()
100-9139

  • Lumbar interspinous decompression instrument set, reusable
Superion Cannula
VERTIFLEX, INC.
N/A
Not in Commercial Distribution

  • 00884662000345 ()
100-9137

  • Lumbar interspinous decompression instrument set, reusable
Superion Dilator 2
VERTIFLEX, INC.
N/A
Not in Commercial Distribution

  • 00884662000338 ()
100-9136

  • Lumbar interspinous decompression instrument set, reusable
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