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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
Izenimplant Co., Ltd.
FDCTM21L
In Commercial Distribution

  • 08800070226568 ()


  • Dental/maxillofacial surgical procedure kit, non-medicated, reusable
No Description
Izenimplant Co., Ltd.
FDCTM21S
In Commercial Distribution

  • 08800070226551 ()


  • Dental/maxillofacial surgical procedure kit, non-medicated, reusable
No Description
Izenimplant Co., Ltd.
FDCSR25L
In Commercial Distribution

  • 08800070226544 ()


  • Dental/maxillofacial surgical procedure kit, non-medicated, reusable
No Description
Izenimplant Co., Ltd.
FDCSR25S
In Commercial Distribution

  • 08800070226537 ()


  • Dental/maxillofacial surgical procedure kit, non-medicated, reusable
No Description
Izenimplant Co., Ltd.
FDCSX17L
In Commercial Distribution

  • 08800070226520 ()


  • Dental/maxillofacial surgical procedure kit, non-medicated, reusable
No Description
Izenimplant Co., Ltd.
FDCSX17S
In Commercial Distribution

  • 08800070226513 ()


  • Dental/maxillofacial surgical procedure kit, non-medicated, reusable
No Description
Izenimplant Co., Ltd.
HEDM1215
In Commercial Distribution

  • 08800070226506 ()


  • Dental/maxillofacial surgical procedure kit, non-medicated, reusable
No Description
Izenimplant Co., Ltd.
HEDM1210
In Commercial Distribution

  • 08800070226490 ()


  • Dental/maxillofacial surgical procedure kit, non-medicated, reusable
No Description
Izenimplant Co., Ltd.
MSADSR20
In Commercial Distribution

  • 08800070226483 ()


  • Dental/maxillofacial surgical procedure kit, non-medicated, reusable
COLUMBUS REV SCREW DRIVER SW3.0
Aesculap AG
NQ642R
In Commercial Distribution

  • 04046963369170 ()
NQ642R

  • Orthopaedic prosthesis implantation positioning instrument, reusable
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