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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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BIORAPTOR 2.9 WITH 2 ULTRABRAID
Smith & Nephew, Inc.
72200775
In Commercial Distribution

  • 03596010585967 ()
72200775

  • Tendon/ligament bone anchor, bioabsorbable
BIORAPTOR 2.9 WITH 1 ULTRABRAID
Smith & Nephew, Inc.
72200774
In Commercial Distribution

  • 03596010585950 ()
72200774

  • Tendon/ligament bone anchor, bioabsorbable
apollo Medial with Needles, 6.5mm
MEDLINE INDUSTRIES, INC.
27-11165
In Commercial Distribution

  • 10818614021376 ()


  • Tendon/ligament bone anchor, non-bioabsorbable
apollo Medial with Needles, 5.5mm
MEDLINE INDUSTRIES, INC.
27-11155
In Commercial Distribution

  • 10818614021369 ()


  • Tendon/ligament bone anchor, non-bioabsorbable
Replacement Set, with anti-luxation device
WALDEMAR LINK GmbH & Co. KG
15-1027/13
In Commercial Distribution

  • 04026575194698 ()
15-1027/13

  • Rotating hinged total knee prosthesis
Replacement Set, with anti-luxation device
WALDEMAR LINK GmbH & Co. KG
15-1027/12
In Commercial Distribution

  • 04026575194681 ()
15-1027/12

  • Rotating hinged total knee prosthesis
Replacement Set, with anti-luxation device
WALDEMAR LINK GmbH & Co. KG
15-1027/11
In Commercial Distribution

  • 04026575194674 ()
15-1027/11

  • Rotating hinged total knee prosthesis
Replacement Set, with anti-luxation device
WALDEMAR LINK GmbH & Co. KG
15-1027/10
In Commercial Distribution

  • 04026575194667 ()
15-1027/10

  • Rotating hinged total knee prosthesis
Dissector Perforator with 13mm tip
KOROS U.S.A., INC.
7222-30
In Commercial Distribution

  • 10840199500168 ()
  • 00840199500161 ()


  • External spinal fixation system
LATERAL,SINGLE LEVEL WITH PROBE
Choice Spine, LP
25-9028
In Commercial Distribution

  • 00840996134897 ()


  • Polymeric spinal interbody fusion cage
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