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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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No Description
SOPRO-COMEG GmbH
395 410 004
In Commercial Distribution

  • 04059082030760 ()


  • Urethral bougie, reusable
No Description
SOPRO-COMEG GmbH
395 410 003
In Commercial Distribution

  • 04059082030753 ()


  • Urethral bougie, reusable
No Description
SOPRO-COMEG GmbH
395 410 002
In Commercial Distribution

  • 04059082030746 ()


  • Urethral bougie, reusable
No Description
SOPRO-COMEG GmbH
395 410 001
In Commercial Distribution

  • 04059082030739 ()


  • Urethral bougie, reusable
No Description
SOPRO-COMEG GmbH
395 410 014BC
In Commercial Distribution

  • 04059082026565 ()


  • Urethral bougie, reusable
No Description
SOPRO-COMEG GmbH
395 410 008BC
In Commercial Distribution

  • 04059082026503 ()


  • Urethral bougie, reusable
No Description
SOPRO-COMEG GmbH
395 410 005BC
In Commercial Distribution

  • 04059082026473 ()


  • Urethral bougie, reusable
No Description
SOPRO-COMEG GmbH
395 410 004BC
In Commercial Distribution

  • 04059082026466 ()


  • Urethral bougie, reusable
No Description
SOPRO-COMEG GmbH
395 410 003BC
In Commercial Distribution

  • 04059082026459 ()


  • Urethral bougie, reusable
No Description
SOPRO-COMEG GmbH
395 410 002BC
In Commercial Distribution

  • 04059082026442 ()


  • Urethral bougie, reusable
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