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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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HTLT Hex Driver .050 ,Tapered, Long
EMERY ENTERPRISES INC
HTLT
In Commercial Distribution

  • 00817686023977 ()


  • Screw endosteal dental implant, two-piece
HNT Hex Driver .048, Short Tapered
EMERY ENTERPRISES INC
HNT
In Commercial Distribution

  • 00817686023946 ()


  • Screw endosteal dental implant, two-piece
HSM Hex Driver .040 Short
EMERY ENTERPRISES INC
HSM
In Commercial Distribution

  • 00817686023922 ()


  • Screw endosteal dental implant, two-piece
MectaLock PEEK Ø3.4 – Long driver
Medacta International SA
05.11.003
In Commercial Distribution

  • 07630040727822 ()


  • Soft-tissue/mesh anchor, non-bioabsorbable
MectaLock PEEK Ø2.9 – Long driver
Medacta International SA
05.11.002
In Commercial Distribution

  • 07630040727815 ()


  • Soft-tissue/mesh anchor, non-bioabsorbable
MectaLock PEEK Ø2.4 – Long driver
Medacta International SA
05.11.001
In Commercial Distribution

  • 07630040727808 ()


  • Soft-tissue/mesh anchor, non-bioabsorbable
MectaLock PEEK Ø3.4 – Short driver
Medacta International SA
05.10.003
In Commercial Distribution

  • 07630040727778 ()


  • Soft-tissue/mesh anchor, non-bioabsorbable
MectaLock PEEK Ø2.9 – Short driver
Medacta International SA
05.10.002
In Commercial Distribution

  • 07630040727761 ()


  • Soft-tissue/mesh anchor, non-bioabsorbable
MectaLock PEEK Ø2.4 – Short driver
Medacta International SA
05.10.001
In Commercial Distribution

  • 07630040727754 ()


  • Soft-tissue/mesh anchor, non-bioabsorbable
Adjustment Instrument LRF
Stryker GmbH
4934-9-100
In Commercial Distribution

  • 07613327072921 ()
4934-9-100

  • External orthopaedic fixation system, reusable
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