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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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RFB ASSY 3.0 SIDEBITER RIGHT
Smith & Nephew, Inc.
7204732D
Not in Commercial Distribution

  • 00885556607312 ()
7204732D

  • Meniscus knife
O*REFURB SMALL JOINT GRASPER
Smith & Nephew, Inc.
013219D
In Commercial Distribution

  • 00885556604540 ()
013219D

  • Meniscus knife
REFURB POSTERIOR PUNCH UPSWEPT
Smith & Nephew, Inc.
012202D
Not in Commercial Distribution

  • 00885556604380 ()
012202D

  • Meniscus knife
REFURB STING RAY LEFT 2.3MM
Smith & Nephew, Inc.
012059D
Not in Commercial Distribution

  • 00885556604373 ()
012059D

  • Meniscus knife
REFURB STING-RAY RIGHT 2.3MM
Smith & Nephew, Inc.
012058D
Not in Commercial Distribution

  • 00885556604366 ()
012058D

  • Meniscus knife
REFURB UPSWEPT BKST PUNCH NARROWLINE
Smith & Nephew, Inc.
012055D
Not in Commercial Distribution

  • 00885556604359 ()
012055D

  • Meniscus knife
REFURB NARROWLINE UPBITER CURVED RT BSKT
Smith & Nephew, Inc.
012054D
Not in Commercial Distribution

  • 00885556604342 ()
012054D

  • Meniscus knife
REFURB NARROWLINE UPBITTER CURVED
Smith & Nephew, Inc.
012053D
Not in Commercial Distribution

  • 00885556604335 ()
012053D

  • Meniscus knife
REFURB DUCKLING STRAIGHT
Smith & Nephew, Inc.
012044D
Not in Commercial Distribution

  • 00885556604298 ()
012044D

  • Meniscus knife
REFURB LINEAR PUNCH SCOOP
Smith & Nephew, Inc.
012033D
Not in Commercial Distribution

  • 00885556604281 ()
012033D

  • Meniscus knife
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