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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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EXPRO 23/3-6-8-11 CC QUALA
NORDENT MANUFACTURING INC
XP23-PC11Q
In Commercial Distribution

  • 00840018602762 ()


  • Dental surgical probe, reusable
PROBE, SE, WILLIAMS, CC QUALA
NORDENT MANUFACTURING INC
PCWQ
In Commercial Distribution

  • 00840018601512 ()


  • Periodontal probe, reusable
PROBE, CC SE 3-6-9-12 QUALA
NORDENT MANUFACTURING INC
PC12Q
In Commercial Distribution

  • 00840018601482 ()


  • Periodontal probe, reusable
PROBE CC SE 3-6-8-11 QUALA
NORDENT MANUFACTURING INC
PC11Q
In Commercial Distribution

  • 00840018601451 ()


  • Periodontal probe, reusable
PROBE, CC, SE, #11.5 QUALA
NORDENT MANUFACTURING INC
P11.5BQ
In Commercial Distribution

  • 00840018601437 ()


  • Periodontal probe, reusable
120mm C-C BLADE, PATLIF RETRACTOR
ALPHATEC SPINE, INC.
169-100-120
In Commercial Distribution

  • 00190376241814 ()


  • Surgical retraction system, reusable
110mm C-C BLADE, PATLIF RETRACTOR
ALPHATEC SPINE, INC.
169-100-110
In Commercial Distribution

  • 00190376241807 ()


  • Surgical retraction system, reusable
100mm C-C BLADE, PATLIF RETRACTOR
ALPHATEC SPINE, INC.
169-100-100
In Commercial Distribution

  • 00190376241791 ()


  • Surgical retraction system, reusable
90mm C-C BLADE, PATLIF RETRACTOR
ALPHATEC SPINE, INC.
169-100-090
In Commercial Distribution

  • 00190376241784 ()


  • Surgical retraction system, reusable
80mm C-C BLADE, PATLIF RETRACTOR
ALPHATEC SPINE, INC.
169-100-080
In Commercial Distribution

  • 00190376241777 ()


  • Surgical retraction system, reusable
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