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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No Description
SIGNATURE ORTHOPAEDICS PTY LTD
122-22-0084
In Commercial Distribution

  • 09348215097417 ()


  • Orthopaedic implant aiming/guiding block, reusable
No Description
SIGNATURE ORTHOPAEDICS PTY LTD
122-22-0083
In Commercial Distribution

  • 09348215097400 ()


  • Orthopaedic implant aiming/guiding block, reusable
No Description
SIGNATURE ORTHOPAEDICS PTY LTD
122-22-0082
In Commercial Distribution

  • 09348215097394 ()


  • Orthopaedic implant aiming/guiding block, reusable
No Description
SIGNATURE ORTHOPAEDICS PTY LTD
122-22-0081
In Commercial Distribution

  • 09348215097387 ()


  • Orthopaedic implant aiming/guiding block, reusable
No Description
SIGNATURE ORTHOPAEDICS PTY LTD
122-22-7000
In Commercial Distribution

  • 09348215097318 ()


  • Orthopaedic implant aiming/guiding block, reusable
No Description
SIGNATURE ORTHOPAEDICS PTY LTD
122-22-0001
In Commercial Distribution

  • 09348215097301 ()


  • Orthopaedic implant aiming/guiding block, reusable
ECONOMY LINE Probe with eye, 5.5", malleable
Avalign Technologies, Inc.
1-11323495
In Commercial Distribution

  • 00190776295561 ()


  • ENT probe, reusable
Lockhart-Mummery Fistula Probe
Avalign Technologies, Inc.
VM21-6717
In Commercial Distribution

  • 00190776213381 ()


  • Fistula probe
Lockhart-Mumery Fistula Probe number 3
Avalign Technologies, Inc.
VM21-6715
In Commercial Distribution

  • 00190776213374 ()


  • Fistula probe
Lockhart-Mumery Fistula Probe number 2
Avalign Technologies, Inc.
VM21-6713
In Commercial Distribution

  • 00190776213367 ()


  • Fistula probe
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