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

  • 00885556608944 ()
7207659F

  • Meniscus knife
REFURB PUNCH SUTURE ACUFEX
Smith & Nephew, Inc.
7207035D
Not in Commercial Distribution

  • 00885556608616 ()
7207035D

  • Meniscus knife
MTO PNCH.BSKT.NRWLN.UPBTR.CRVD RT.
Smith & Nephew, Inc.
3134042
Not in Commercial Distribution

  • 00885556658079 ()
3134042

  • Meniscus knife
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
MTO SCOOP PROLINE 2.7MM
Smith & Nephew, Inc.
72202212
In Commercial Distribution

  • 00885554016314 ()
72202212

  • Meniscus knife
MTO UPBITER BLUNT NOSE JR.
Smith & Nephew, Inc.
72202058
Not in Commercial Distribution

  • 00885554015072 ()
72202058

  • Meniscus knife
SOD DUCKBILL BSKT PNCH REV UPBITER
Smith & Nephew, Inc.
7210489
In Commercial Distribution

  • 00885554012705 ()
7210489

  • Meniscus knife
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