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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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IBAL PFJ,POST REFERENCING GD
ARTHREX, INC.
AR-602-7
Not in Commercial Distribution

  • 00888867111417 ()
AR-602-7

  • Surgical drill guide, reusable
UKA TIBIA CUT CORRECTION GUIDE, 2MM
ARTHREX, INC.
AR-601-TCCG-2
In Commercial Distribution

  • 00888867111301 ()
AR-601-TCCG-2

  • Surgical drill guide, reusable
DOUBLE BUNDLE PCL GUIDE SET
ARTHREX, INC.
AR-5015S
In Commercial Distribution

  • 00888867102705 ()
AR-5015S

  • Orthopaedic surgical procedure kit, non-medicated, reusable
DISPOSABLES KIT FOR 2.9MM SHORT PUSHLOCK
ARTHREX, INC.
AR-2923DS
In Commercial Distribution

  • 00888867099210 ()
AR-2923DS

  • Arthroscopic surgical procedure kit, non-medicated, single-use
6 3/4 Inch Miller Rectal Scissors, Double Curved, Blunt, Serrated
Surgical Direct, Inc.
SD90324210
In Commercial Distribution

  • B382SD903242100 ()
SD90324210

  • Rectal speculum
11MM TENDON STRIPPER BLADE
ARTHREX, INC.
AR-2385-11
In Commercial Distribution

  • 10888867098272 ()
  • 00888867098275 ()
AR-2385-11

  • Tendon stripper
10MM TENDON STRIPPER BLADE
ARTHREX, INC.
AR-2385-10
In Commercial Distribution

  • 10888867098265 ()
  • 00888867098268 ()
AR-2385-10

  • Tendon stripper
9MM TENDON STRIPPER BLA
ARTHREX, INC.
AR-2385-09
In Commercial Distribution

  • 10888867098258 ()
  • 00888867098251 ()
AR-2385-09

  • Tendon stripper
QUAD TENDON STRIPPER- CUTTER
ARTHREX, INC.
AR-2384
In Commercial Distribution

  • 00888867098244 ()
AR-2384

  • Tendon stripper
QUAD TENDON GRAFT CUTTING GUIDE
ARTHREX, INC.
AR-2383
In Commercial Distribution

  • 00888867098237 ()
AR-2383

  • Orthopaedic graft guide
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