SEARCH RESULTS FOR: 万事达u卡app(www.usdtcard.org)hoGq(3380 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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TAYLOR SPATIAL FRAME U PLATE 105MM INNER DIAMETER with ADDITIONAL HOLES
Smith & Nephew, Inc.
71071302
In Commercial Distribution

  • 03596010571410 ()
71071302

  • External orthopaedic fixation system, single-use
TAYLOR SPATIAL FRAME U PLATE 80MM INNER DIAMETER with ADDITIONAL HOLES
Smith & Nephew, Inc.
71071301
In Commercial Distribution

  • 03596010571403 ()
71071301

  • External orthopaedic fixation system, single-use
Connector, Lateral Offset, 4.75/6.0 (U), 5.5 mm x 40 mm
Spine Wave, Inc.
11-7939
In Commercial Distribution

  • 10840642158663 ()


  • Bone-screw internal spinal fixation system connector
Connector, Lateral Offset, 4.75/6.0 (U), 5.5 mm x 30 mm
Spine Wave, Inc.
11-7938
In Commercial Distribution

  • 10840642158656 ()


  • Bone-screw internal spinal fixation system connector
Connector, Lateral Offset, 4.75/6.0 (U), 5.5 mm x 20 mm
Spine Wave, Inc.
11-7937
In Commercial Distribution

  • 10840642158649 ()


  • Bone-screw internal spinal fixation system connector
Single Offset Connector, 3.5/4.0(U), 4.0 mm Rod × 11 mm
Spine Wave, Inc.
11-9243
In Commercial Distribution

  • 10840642121339 ()
11-9243

  • Bone-screw internal spinal fixation system connector
Double Offset Connector, 3.5/4.0(U), 4.0 mm Rod × 11 mm
Spine Wave, Inc.
11-9238
In Commercial Distribution

  • 10840642121285 ()
11-9238

  • Bone-screw internal spinal fixation system connector
Single Offset Connector, 3.5/4.0(U), 4.0 mm Rod × 21 mm
Spine Wave, Inc.
11-9233
In Commercial Distribution

  • 10840642121230 ()
11-9233

  • Bone-screw internal spinal fixation system connector
Double Offset Connector, 3.5/4.0(U), 4.0 mm Rod × 21 mm
Spine Wave, Inc.
11-9227
In Commercial Distribution

  • 10840642121179 ()
11-9227

  • Bone-screw internal spinal fixation system connector
B-P KNEE TIBIA PLATFORM COMPONENT, W/O BIOCOAT, W/ULTRACOAT, TYPE 0, SIZE 2 https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml#
ENDOTEC, INC.
04-32-0462
Not in Commercial Distribution

  • 00814193021519 ()

  • SIZE 2, TYPE 0
04-32-0462

  • Cruciate-retaining total knee prosthesis
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