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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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26x35x13, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-M130
In Commercial Distribution

  • B0621750M130 ()
1750-M130

  • Surgical instrument/implant depth limiter, reusable
26x35x11, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-M110
In Commercial Distribution

  • B0621750M110 ()
1750-M110

  • Surgical instrument/implant depth limiter, reusable
29x39x19, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-L190
In Commercial Distribution

  • B0621750L190 ()
1750-L190

  • Surgical instrument/implant depth limiter, reusable
29x39x15, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-L150
In Commercial Distribution

  • B0621750L150 ()
1750-L150

  • Surgical instrument/implant depth limiter, reusable
29x39x13, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-L130
In Commercial Distribution

  • B0621750L130 ()
1750-L130

  • Surgical instrument/implant depth limiter, reusable
29x39x11, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-L110
In Commercial Distribution

  • B0621750L110 ()
1750-L110

  • Surgical instrument/implant depth limiter, reusable
Channels K-Files 25mm, #20
HENRY SCHEIN, INC.
2020094
In Commercial Distribution

  • 10304040039127 ()
  • 00304040039120 ()

  • Outer Diameter: 0.2 Millimeter
2020094

  • Manual endodontic file/rasp, reusable
Channels K-Files 21mm, #20
HENRY SCHEIN, INC.
2020075
In Commercial Distribution

  • 10304040038076 ()
  • 00304040038079 ()

  • Outer Diameter: 0.2 Millimeter
2020075

  • Manual endodontic file/rasp, reusable
Mini Curette, Large, 20°
Paragon 28, Inc.
P99-150-0091
In Commercial Distribution

  • 00889795041050 ()
P99-150-0091

  • Bone curette, reusable
Mixing tips type 20
VOCO GmbH
2202
In Commercial Distribution

  • E22122021 ()
  • E2212202 ()


  • Dental material mixing nozzle
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