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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
UNIVERDERM
Lidocaine
In Commercial Distribution

  • 03770034301097 ()
  • 03770034301103 ()


  • Dermal tissue reconstructive material, microbe-derived, anaesthetic
No Description
UNIVERDERM
Lidocaine
In Commercial Distribution

  • 03770034301066 ()


  • Dermal tissue reconstructive material, microbe-derived, anaesthetic
No Description
UNIVERDERM
Defyne with Lidocaine
In Commercial Distribution

  • 03770034301059 ()


  • Dermal tissue reconstructive material, microbe-derived, anaesthetic
No Description
UNIVERDERM
Kysse with Lidocaine
In Commercial Distribution

  • 03770034301042 ()


  • Dermal tissue reconstructive material, microbe-derived, anaesthetic
No Description
UNIVERDERM
Lyft Lidocaine
In Commercial Distribution

  • 03770034301035 ()


  • Dermal tissue reconstructive material, microbe-derived, anaesthetic
No Description
UNIVERDERM
Refyne with Lidocaine
In Commercial Distribution

  • 03770034301028 ()


  • Dermal tissue reconstructive material, microbe-derived, anaesthetic
No Description
UNIVERDERM
Voluma
In Commercial Distribution

  • 03770034301011 ()
  • 03770034301073 ()


  • Dermal tissue reconstructive material, microbe-derived, anaesthetic
No Description
UNIVERDERM
Volbella
In Commercial Distribution

  • 03770034301004 ()
  • 03770034301080 ()


  • Dermal tissue reconstructive material, microbe-derived, anaesthetic
EOlife Charger (ref: A0000029) it the charger of the final device EOlife (AUS00055)
ARCHEON
A0000029
In Commercial Distribution

  • 03770016085076 ()


  • Pulmonary resuscitator, manual, reusable
EOlife ECU (ref: AUS00004) is the Electronic Control Unit of the EOlife device (ref: AUS00055).
ARCHEON
AUS00004
In Commercial Distribution

  • 03770016085052 ()


  • Pulmonary resuscitator, manual, reusable
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