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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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COURTESY TIE TO SAN31NEUIA PK
Cardinal Health 200, LLC
SID31NEUIA
In Commercial Distribution

  • 50887488618591 ()
  • 10887488618593 ()
SID31NEUIA

  • General surgical procedure kit, non-medicated, single-use
Designed to remove pulp tissue.
DiaDent Group International
25m/m 25/40(XXXF/F)
In Commercial Distribution

  • 08806383520584 ()
504-292

  • Endodontic broach, serrated, reusable
Designed to remove pulp tissue.
DiaDent Group International
25m/m 40(F)
In Commercial Distribution

  • 08806383520577 ()
504-205

  • Endodontic broach, serrated, reusable
Designed to remove pulp tissue.
DiaDent Group International
25m/m 35(XF)
In Commercial Distribution

  • 08806383520560 ()
504-204

  • Endodontic broach, serrated, reusable
Designed to remove pulp tissue.
DiaDent Group International
25m/m 30(XXF)
In Commercial Distribution

  • 08806383520553 ()
504-203

  • Endodontic broach, serrated, reusable
Designed to remove pulp tissue.
DiaDent Group International
25m/m 25(XXXF)
In Commercial Distribution

  • 08806383520546 ()
504-202

  • Endodontic broach, serrated, reusable
Designed to remove pulp tissue.
DiaDent Group International
25m/m 20(XXXXF)
In Commercial Distribution

  • 08806383520539 ()
504-201

  • Endodontic broach, serrated, reusable
Designed to remove pulp tissue.
DiaDent Group International
21m/m 25/40(XXXF/F)
In Commercial Distribution

  • 08806383520522 ()
504-092

  • Endodontic broach, serrated, reusable
Designed to remove pulp tissue.
DiaDent Group International
21m/m 25/60(XXXF/C)
In Commercial Distribution

  • 08806383520515 ()
504-091

  • Endodontic broach, serrated, reusable
Designed to remove pulp tissue.
DiaDent Group International
21m/m 60(C)
In Commercial Distribution

  • 08806383520508 ()
504-007

  • Endodontic broach, serrated, reusable
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