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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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FORCEPS WITH WINDOW
HOYA CORPORATION
KW3122S
Not in Commercial Distribution

  • 04961333224708 ()
  • 04961333071029 ()


  • Open-surgery biopsy forceps, reusable
FORCEPS WITH WINDOW
HOYA CORPORATION
KW3115S
Not in Commercial Distribution

  • 04961333224685 ()
  • 04961333083428 ()


  • Open-surgery biopsy forceps, reusable
FORCEPS WITH WINDOW
HOYA CORPORATION
KW3111S
Not in Commercial Distribution

  • 04961333224661 ()
  • 04961333083411 ()


  • Open-surgery biopsy forceps, reusable
FORCEPS WITH WINDOW
HOYA CORPORATION
KW2422S
Not in Commercial Distribution

  • 04961333224623 ()
  • 04961333071012 ()


  • Open-surgery biopsy forceps, reusable
FORCEPS WITH WINDOW
HOYA CORPORATION
KW2411S
Not in Commercial Distribution

  • 04961333224562 ()
  • 04961333070985 ()


  • Open-surgery biopsy forceps, reusable
FORCEPS WITH WINDOW
HOYA CORPORATION
KW2218CS
Not in Commercial Distribution

  • 04961333224548 ()
  • 04961333083404 ()


  • Open-surgery biopsy forceps, reusable
FORCEPS WITH WINDOW
HOYA CORPORATION
KW2211S
Not in Commercial Distribution

  • 04961333224500 ()
  • 04961333083435 ()


  • Open-surgery biopsy forceps, reusable
FORCEPS WITH WINDOW
HOYA CORPORATION
KW1818CS
Not in Commercial Distribution

  • 04961333224463 ()
  • 04961333136421 ()


  • Open-surgery biopsy forceps, reusable
FORCEPS WITH WINDOW
HOYA CORPORATION
KW1811S
Not in Commercial Distribution

  • 04961333224425 ()
  • 04961333070961 ()


  • Open-surgery biopsy forceps, reusable
CENTESIS WITH TURKEL
Cardinal Health 200, LLC
30-0307K
In Commercial Distribution

  • 50888439873021 ()
  • 10888439873023 ()
30-0307K

  • General surgical procedure kit, medicated
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