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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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TRIAL, CC SPINE, SIZE 1 DELTA
Exactech, Inc.
209-52-10
In Commercial Distribution

  • 10885862056498 ()

  • SIZE 1
209-52-10

  • Knee tibia prosthesis trial, reusable
FEMORAL FINISHING GUIDE, CC, SIZE 5
Exactech, Inc.
209-51-05
In Commercial Distribution

  • 10885862056382 ()

  • SIZE 5
209-51-05

  • Osteotomy guide, reusable
FEMORAL FINISHING GUIDE, CC, SIZE 4
Exactech, Inc.
209-51-04
In Commercial Distribution

  • 10885862056375 ()

  • SIZE 4
209-51-04

  • Osteotomy guide, reusable
FEMORAL FINISHING GUIDE, CC, SIZE 3
Exactech, Inc.
209-51-03
In Commercial Distribution

  • 10885862056368 ()

  • SIZE 3
209-51-03

  • Osteotomy guide, reusable
FEMORAL FINISHING GUIDE, CC, SIZE 2
Exactech, Inc.
209-51-02
In Commercial Distribution

  • 10885862056351 ()

  • SIZE 2
209-51-02

  • Osteotomy guide, reusable
FEMORAL FINISHING GUIDE, CC, SIZE 1
Exactech, Inc.
209-51-01
In Commercial Distribution

  • 10885862056344 ()

  • SIZE 1
209-51-01

  • Osteotomy guide, reusable
FEMORAL LATERAL TEMPLATE, CC, SIZE 5
Exactech, Inc.
209-47-05
In Commercial Distribution

  • 10885862056337 ()

  • SIZE 5
209-47-05

  • Surgical implant template, reusable
FEMORAL LATERAL TEMPLATE, CC, SIZE 4
Exactech, Inc.
209-47-04
In Commercial Distribution

  • 10885862056320 ()

  • SIZE 4
209-47-04

  • Surgical implant template, reusable
TRIAL, CC FEMORAL, OPTIMIZED, SIZE 5
Exactech, Inc.
209-01-15
In Commercial Distribution

  • 10885862054654 ()

  • SIZE 5
209-01-15

  • Knee femur prosthesis trial, reusable
TRIAL, CC FEMORAL, OPTIMIZED, SIZE 4
Exactech, Inc.
209-01-14
In Commercial Distribution

  • 10885862054647 ()

  • SIZE 4
209-01-14

  • Knee femur prosthesis trial, reusable
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