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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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TI MATRIXNEURO Y-PLATE 5 HOLES
Synthes GmbH
04.503.067
In Commercial Distribution

  • H980045030670 ()
  • 10887587017990 ()
04503067

  • Craniofacial fixation plate, non-bioabsorbable, non-customized
Cup Curette Size 5 Forward
Evolution Spine LLC
111-A115
In Commercial Distribution

  • 00195860020203 ()
111-A115

  • General-purpose curette
Cup Curette Size 5 Reverse
Evolution Spine LLC
111-A114
In Commercial Distribution

  • 00195860020197 ()
111-A114

  • General-purpose curette
Cup Curette Size 5 Straight
Evolution Spine LLC
111-A113
In Commercial Distribution

  • 00195860020180 ()
111-A113

  • General-purpose curette
PLATE, TMT STRAIGHT, 5 HOLE
MEDLINE INDUSTRIES, INC.
MPP3005U
In Commercial Distribution

  • 10888277364189 ()
MPP3005U

  • Orthopaedic fixation plate, non-bioabsorbable
TELIX K Trial 8x32mm, 5°
Biedermann Motech GmbH & Co. KG
209-050-0110
In Commercial Distribution

  • 04250869608008 ()
209-050-0110

  • General internal orthopaedic fixation system implantation kit
TELIX K Trial 13x28mm, 5°
Biedermann Motech GmbH & Co. KG
209-050-0108
In Commercial Distribution

  • 04250869607988 ()
209-050-0108

  • General internal orthopaedic fixation system implantation kit
TELIX K Trial 12x28mm, 5°
Biedermann Motech GmbH & Co. KG
209-050-0107
In Commercial Distribution

  • 04250869607971 ()
209-050-0107

  • General internal orthopaedic fixation system implantation kit
TELIX K Trial 11x28mm, 5°
Biedermann Motech GmbH & Co. KG
209-050-0106
In Commercial Distribution

  • 04250869607964 ()
209-050-0106

  • General internal orthopaedic fixation system implantation kit
TELIX K Trial 10x28mm, 5°
Biedermann Motech GmbH & Co. KG
209-050-0105
In Commercial Distribution

  • 04250869607940 ()
209-050-0105

  • General internal orthopaedic fixation system implantation kit
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