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

  • 00885556604373 ()
012059D

  • Meniscus knife
MTO PUNCH BASKET 45 ROTARY L
Smith & Nephew, Inc.
7209890
Not in Commercial Distribution

  • 00885556603208 ()
7209890

  • Meniscus knife
MTO PUNCH BASKET 45 ROTARY RIGHT
Smith & Nephew, Inc.
7209889
Not in Commercial Distribution

  • 00885556603192 ()
7209889

  • Meniscus knife
SOD PCH CAPSULAR RELEASE 15
Smith & Nephew, Inc.
6900910
Not in Commercial Distribution

  • 00885556601365 ()
6900910

  • Meniscus knife
SOD PCH CAPSULAR RELEASE 15
Smith & Nephew, Inc.
6900909
Not in Commercial Distribution

  • 00885556601358 ()
6900909

  • Meniscus knife
MTO PCH OVAL CRVD L 40MM TOP LEVEL ASSY
Smith & Nephew, Inc.
3134238
Not in Commercial Distribution

  • 00885556600450 ()
3134238

  • Meniscus knife
SOD PUNCH SCOOP STRT 1.0MM
Smith & Nephew, Inc.
3134076
Not in Commercial Distribution

  • 00885556600122 ()
3134076

  • Meniscus knife
REFURBISHED PNCH MENISCAL ELEV 1.3 W/PR
Smith & Nephew, Inc.
7207671F
Not in Commercial Distribution

  • 00885556608951 ()
7207671F

  • Meniscus knife
REFURBISHED PNCH NARROWLINE UPSWEPT W/PR
Smith & Nephew, Inc.
7207659F
Not in Commercial Distribution

  • 00885556608944 ()
7207659F

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

  • 00885556604540 ()
013219D

  • Meniscus knife
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