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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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CC FEMORAL FINISHING GUIDE SIZE 5
Exactech, Inc.
02-019-50-0150
In Commercial Distribution

  • 10885862286086 ()

  • SIZE 5
02-019-50-0150

  • Osteotomy guide, reusable
CC FEMORAL FINISHING GUIDE SIZE 4
Exactech, Inc.
02-019-50-0140
In Commercial Distribution

  • 10885862286079 ()

  • SIZE 4
02-019-50-0140

  • Osteotomy guide, reusable
CC FEMORAL FINISHING GUIDE SIZE 3
Exactech, Inc.
02-019-50-0130
In Commercial Distribution

  • 10885862286062 ()

  • SIZE 3
02-019-50-0130

  • Osteotomy guide, reusable
CC FEMORAL FINISHING GUIDE SIZE 2
Exactech, Inc.
02-019-50-0120
In Commercial Distribution

  • 10885862286055 ()

  • SIZE 2
02-019-50-0120

  • Osteotomy guide, reusable
CC FEMORAL FINISHING GUIDE SIZE 1
Exactech, Inc.
02-019-50-0110
In Commercial Distribution

  • 10885862286048 ()

  • SIZE 1
02-019-50-0110

  • Osteotomy guide, reusable
FEMORAL NOTCH GUIDE, CC, SIZE 5
Exactech, Inc.
209-53-05
In Commercial Distribution

  • 10885862056559 ()

  • SIZE 5
209-53-05

  • Osteotomy guide, reusable
FEMORAL NOTCH GUIDE, CC, SIZE 4
Exactech, Inc.
209-53-04
In Commercial Distribution

  • 10885862056542 ()

  • SIZE 4
209-53-04

  • Osteotomy guide, reusable
FEMORAL NOTCH GUIDE, CC, SIZE 3
Exactech, Inc.
209-53-03
In Commercial Distribution

  • 10885862056535 ()

  • SIZE 3
209-53-03

  • Osteotomy guide, reusable
FEMORAL NOTCH GUIDE, CC, SIZE 2
Exactech, Inc.
209-53-02
In Commercial Distribution

  • 10885862056528 ()

  • SIZE 2
209-53-02

  • Osteotomy guide, reusable
FEMORAL NOTCH GUIDE, CC, SIZE 1
Exactech, Inc.
209-53-01
In Commercial Distribution

  • 10885862056511 ()

  • SIZE 1
209-53-01

  • Osteotomy guide, reusable
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