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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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PROBE BLUNT - STRAIGHT
SpineArt SA
TLF-IN 01 30-N
In Commercial Distribution

  • 07640185349148 ()
TLF-IN 01 30-N

  • Bone awl, reusable
PROBE SMALL - CURVED
SpineArt SA
TLF-IN 01 20-N
In Commercial Distribution

  • 07640185349131 ()
TLF-IN 01 20-N

  • Bone awl, reusable
PROBE - CURVED
SpineArt SA
TLF-IN 01 10-N
In Commercial Distribution

  • 07640185349124 ()
TLF-IN 01 10-N

  • Bone awl, reusable
BONE AWL
SpineArt SA
TLF-IN 00 00-N
In Commercial Distribution

  • 07640185349117 ()
TLF-IN 00 00-N

  • Bone awl, reusable
BEVELED ANGLED AWL
SpineArt SA
SPE-US 00 52-N
In Commercial Distribution

  • 07640185349032 ()

  • Outer Diameter: 4.5 Millimeter
SPE-US 00 52-N

  • Bone awl, reusable
BEVELED STRAIGHT AWL
SpineArt SA
SPE-US 00 51-N
In Commercial Distribution

  • 07640185349025 ()

  • Outer Diameter: 4.5 Millimeter
SPE-US 00 51-N

  • Bone awl, reusable
BALL TIP PROBE
SpineArt SA
SCA-IN 20 00-N
In Commercial Distribution

  • 07640185340770 ()
SCA-IN 20 00-N

  • Bone awl, reusable
ANGLED SQUARE AWL
SpineArt SA
SJT-IN 01 01-N
In Commercial Distribution

  • 07640185340039 ()
SJT-IN 01 01-N

  • Bone awl, reusable
STRAIGHT SQUARE AWL
SpineArt SA
SJT-IN 01 00-N
In Commercial Distribution

  • 07640185340022 ()
SJT-IN 01 00-N

  • Bone awl, reusable
CANNULATED BONE AWL
SpineArt SA
ELL-IN 01 01-N
In Commercial Distribution

  • 07640178989375 ()
ELL-IN 01 01-N

  • Bone awl, reusable
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