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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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ROTATE CUTTER, 8MM
TITAN SPINE, LLC
7200-1019
Not in Commercial Distribution

  • M682720010190 ()

  • Width: 8 Millimeter
  • Length: 16 Inch
7200-1019

  • Bone curette, reusable
Cone Ring Curette #3, Straight
TITAN SPINE, LLC
711-1503-0
Not in Commercial Distribution

  • M682711150300 ()
711-1503-0

  • Bone curette, reusable
Long Curette #6, 18in Length, 9in Handle, Angled
TITAN SPINE, LLC
710-1806-1
Not in Commercial Distribution

  • M682710180610 ()
710-1806-1

  • Bone curette, reusable
Long Curette #4, 18in Length, 9in Handle, Angled
TITAN SPINE, LLC
710-1804-1
Not in Commercial Distribution

  • M682710180410 ()
710-1804-1

  • Bone curette, reusable
Long Curette #2, 18in Length, 9in Handle, Angled
TITAN SPINE, LLC
710-1802-1
Not in Commercial Distribution

  • M682710180210 ()
710-1802-1

  • Bone curette, reusable
Long Curette #6, 15in Length, 9in Handle
TITAN SPINE, LLC
710-1506-0
Not in Commercial Distribution

  • M682710150600 ()
710-1506-0

  • Bone curette, reusable
Long Curette #4, 15in Length, 9in Handle
TITAN SPINE, LLC
710-1504-0
Not in Commercial Distribution

  • M682710150400 ()
710-1504-0

  • Bone curette, reusable
Long Curette #2, 15in Length, 9in Handle
TITAN SPINE, LLC
710-1502-0
Not in Commercial Distribution

  • M682710150200 ()
710-1502-0

  • Bone curette, reusable
VAGINAL SPECULUM WITH LIGHT SOURCE SINGLE-USE SIZE LARGE
OBP CORPORATION
C020520
In Commercial Distribution

  • M648C0205202 ()
  • M648C0205201 ()
  • M648C0205200 ()


  • Vaginal speculum, single-use
VAGINAL SPECULUM WITH LIGHT SOURCE SINGLE-USE SIZE MEDIUM
OBP CORPORATION
C020510
In Commercial Distribution

  • M648C0205102 ()
  • M648C0205101 ()
  • M648C0205100 ()


  • Vaginal speculum, single-use
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