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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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icotec Lumbar Cage PLIF 8° / 25 mm x 12 mm
icotec AG
13-59-82512
In Commercial Distribution

  • 07640164848426 ()
13-59-82512

  • Polymeric spinal interbody fusion cage
icotec Lumbar Cage PLIF 8° / 25 mm x 11 mm
icotec AG
13-59-82511
In Commercial Distribution

  • 07640164848419 ()
13-59-82511

  • Polymeric spinal interbody fusion cage
icotec Lumbar Cage PLIF 8° / 25 mm x 09 mm
icotec AG
13-59-82509
In Commercial Distribution

  • 07640164848396 ()
13-59-82509

  • Polymeric spinal interbody fusion cage
icotec Lumbar Cage PLIF 4° / 25 mm x 15 mm
icotec AG
13-59-42515
In Commercial Distribution

  • 07640164848389 ()
13-59-42515

  • Polymeric spinal interbody fusion cage
icotec Lumbar Cage PLIF 4° / 25 mm x 13 mm
icotec AG
13-59-42513
In Commercial Distribution

  • 07640164848365 ()
13-59-42513

  • Polymeric spinal interbody fusion cage
icotec Lumbar Cage PLIF 4° / 25 mm x 11 mm
icotec AG
13-59-42511
In Commercial Distribution

  • 07640164848341 ()
13-59-42511

  • Polymeric spinal interbody fusion cage
icotec Lumbar Cage PLIF 4° / 25 mm x 09 mm
icotec AG
13-59-42509
In Commercial Distribution

  • 07640164848327 ()
13-59-42509

  • Polymeric spinal interbody fusion cage
icotec Lumbar Cage PLIF 4° / 25 mm x 07 mm
icotec AG
13-59-42507
In Commercial Distribution

  • 07640164848303 ()
13-59-42507

  • Polymeric spinal interbody fusion cage
icotec Lumbar Cage PLIF 0° / 25 mm x 15 mm
icotec AG
13-59-02515
In Commercial Distribution

  • 07640164848297 ()
13-59-02515

  • Polymeric spinal interbody fusion cage
icotec Lumbar Cage PLIF 0° / 25 mm x 13 mm
icotec AG
13-59-02513
In Commercial Distribution

  • 07640164848273 ()
13-59-02513

  • Polymeric spinal interbody fusion cage
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