SEARCH RESULTS FOR: Femoral(15990 results)

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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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Femoral A/P chamfer resection guide, AR, #6
UNITED ORTHOPEDIC CORP.
9304-2460
In Commercial Distribution

  • 04719886890228 ()
9304-2460

  • Osteotomy guide, reusable
Femoral A/P chamfer resection guide, AR, #5.5
UNITED ORTHOPEDIC CORP.
9304-2455
In Commercial Distribution

  • 04719886890211 ()
9304-2455

  • Osteotomy guide, reusable
Femoral A/P chamfer resection guide, AR, #5
UNITED ORTHOPEDIC CORP.
9304-2450
In Commercial Distribution

  • 04719886890204 ()
9304-2450

  • Osteotomy guide, reusable
Femoral A/P chamfer resection guide, AR, #4.5
UNITED ORTHOPEDIC CORP.
9304-2445
In Commercial Distribution

  • 04719886890198 ()
9304-2445

  • Osteotomy guide, reusable
Femoral A/P chamfer resection guide, PR, #7
UNITED ORTHOPEDIC CORP.
9304-2670
In Commercial Distribution

  • 04719886890372 ()
9304-2670

  • Osteotomy guide, reusable
Femoral A/P chamfer resection guide, PR, #6.5
UNITED ORTHOPEDIC CORP.
9304-2665
In Commercial Distribution

  • 04719886890365 ()
9304-2665

  • Osteotomy guide, reusable
Femoral A/P chamfer resection guide, PR, #6
UNITED ORTHOPEDIC CORP.
9304-2660
In Commercial Distribution

  • 04719886890358 ()
9304-2660

  • Osteotomy guide, reusable
Femoral A/P chamfer resection guide, PR, #5.5
UNITED ORTHOPEDIC CORP.
9304-2655
In Commercial Distribution

  • 04719886890341 ()
9304-2655

  • Osteotomy guide, reusable
Femoral A/P chamfer resection guide, PR, #5
UNITED ORTHOPEDIC CORP.
9304-2650
In Commercial Distribution

  • 04719886890334 ()
9304-2650

  • Osteotomy guide, reusable
Femoral A/P chamfer resection guide, PR, #4.5
UNITED ORTHOPEDIC CORP.
9304-2645
In Commercial Distribution

  • 04719886890327 ()
9304-2645

  • Osteotomy guide, reusable
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