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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 001BC
In Commercial Distribution

  • 04059082026435 ()


  • Urethral bougie, reusable
No Description
SOPRO-COMEG GmbH
395 410 018BC
In Commercial Distribution

  • 04059082026602 ()


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

  • 04059082026596 ()


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

  • 04059082026589 ()


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

  • 04059082026572 ()


  • Urethral bougie, reusable
No Description
SOPRO-COMEG GmbH
395 410 013BC
In Commercial Distribution

  • 04059082026558 ()


  • Urethral bougie, reusable
No Description
SOPRO-COMEG GmbH
395 410 012BC
In Commercial Distribution

  • 04059082026541 ()


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

  • 04059082026534 ()


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

  • 04059082026527 ()


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

  • 04059082026510 ()


  • Urethral bougie, reusable
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