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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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Sterile Parcus Braid 5 w/ Needles
PARCUS MEDICAL LLC
20059
In Commercial Distribution

  • M685200591 ()
  • M685200590 ()
20059

  • Polyolefin/fluoropolymer suture, multifilament
Rasp, 10 deg, 5&6 mm
Zavation LLC
20-2004-05
In Commercial Distribution

  • 00842166177789 ()


  • Polymeric spinal interbody fusion cage
Rasp, 6 deg, 5&6 mm
Zavation LLC
20-2004-01
In Commercial Distribution

  • 00842166177741 ()


  • Polymeric spinal interbody fusion cage
TI MATRIXNEURO ADAPTION PLATE 5 HOLES
Synthes GmbH
04.503.070
In Commercial Distribution

  • H980045030700 ()
  • 10887587018027 ()
04503070

  • Craniofacial fixation plate, non-bioabsorbable, non-customized
TELIX K Ti Cage 17x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1736
In Commercial Distribution

  • 04250869607872 ()
109-015-1736

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 16x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1636
In Commercial Distribution

  • 04250869607865 ()
109-015-1636

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 15x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1536
In Commercial Distribution

  • 04250869607858 ()
109-015-1536

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 14x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1436
In Commercial Distribution

  • 04250869607841 ()
109-015-1436

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 13x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1336
In Commercial Distribution

  • 04250869607834 ()
109-015-1336

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 12x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1236
In Commercial Distribution

  • 04250869607827 ()
109-015-1236

  • Metallic spinal interbody fusion cage
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