SEARCH RESULTS FOR: 仿制AT(557058 results)

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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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KMEDIC - 24026704272703

SMILLIE KNIFE STRAIGHT
TELEFLEX INCORPORATED
IPN014005
In Commercial Distribution

  • 24026704272703 ()
  • 04026704272709 ()

  • Length: 15.8 Centimeter
KM46762

  • Meniscus knife

N/A - 00885556658079

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

  • 00885556658079 ()
3134042

  • Meniscus knife

N/A - 00885556608951

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

  • 00885556608951 ()
7207671F

  • Meniscus knife

N/A - 00885556608944

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

  • 00885556608944 ()
7207659F

  • Meniscus knife

ACUFEX - 00885556608616

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

  • 00885556608616 ()
7207035D

  • Meniscus knife

N/A - 00885556607312

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

  • 00885556607312 ()
7204732D

  • Meniscus knife

ACUFEX - 00885556604540

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

  • 00885556604540 ()
013219D

  • Meniscus knife

N/A - 00885556604380

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

  • 00885556604380 ()
012202D

  • Meniscus knife

N/A - 00885556604373

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

  • 00885556604373 ()
012059D

  • Meniscus knife

N/A - 00885556604366

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

  • 00885556604366 ()
012058D

  • Meniscus knife
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