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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
395 410 012
In Commercial Distribution

  • 04059082030838 ()


  • Urethral bougie, reusable
No Description
SOPRO-COMEG GmbH
395 410 011
In Commercial Distribution

  • 04059082030821 ()


  • Urethral bougie, reusable
No Description
SOPRO-COMEG GmbH
395 410 010
In Commercial Distribution

  • 04059082030814 ()


  • Urethral bougie, reusable
No Description
SOPRO-COMEG GmbH
395 410 009
In Commercial Distribution

  • 04059082030807 ()


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

  • 04059082030791 ()


  • Urethral bougie, reusable
No Description
SOPRO-COMEG GmbH
395 410 007
In Commercial Distribution

  • 04059082030784 ()


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

  • 04059082030777 ()


  • Urethral bougie, reusable
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
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