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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 007BC
In Commercial Distribution

  • 04059082026497 ()


  • 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
No Description
SOPRO-COMEG GmbH
395 410 018
In Commercial Distribution

  • 04059082030890 ()


  • Urethral bougie, reusable
No Description
SOPRO-COMEG GmbH
395 410 017
In Commercial Distribution

  • 04059082030883 ()


  • Urethral bougie, reusable
No Description
SOPRO-COMEG GmbH
395 410 016
In Commercial Distribution

  • 04059082030876 ()


  • Urethral bougie, reusable
No Description
SOPRO-COMEG GmbH
395 410 015
In Commercial Distribution

  • 04059082030869 ()


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

  • 04059082030852 ()


  • Urethral bougie, reusable
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