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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 MICROPUNCH TEARDROP LEFT
Smith & Nephew, Inc.
7207602D
In Commercial Distribution

  • 00885556504635 ()
7207602D

  • Meniscus knife
REFURB MICROGRASPER UPBITER
Smith & Nephew, Inc.
7207599D
Not in Commercial Distribution

  • 00885556504628 ()
7207599D

  • Meniscus knife
REFURB PCH OVAL STR
Smith & Nephew, Inc.
7207201D
Not in Commercial Distribution

  • 00885556504574 ()
7207201D

  • Meniscus knife
REFURB.PCH OVAL UPBTR 15D
Smith & Nephew, Inc.
7207200D
Not in Commercial Distribution

  • 00885556504567 ()
7207200D

  • Meniscus knife
SOD PUNCH DUCKLING UPSIDE DOWN
Smith & Nephew, Inc.
6901123
Not in Commercial Distribution

  • 00885556601990 ()
6901123

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

  • 00885556608951 ()
7207671F

  • Meniscus knife
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
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