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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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U2 Tibial insert, PS, #5, 13mm
UNITED ORTHOPEDIC CORP.
2303-3053
In Commercial Distribution

  • 04712602348225 ()

  • 13mm
2303-3053

  • Posterior-stabilized total knee prosthesis
U2 Tibial insert, PS, #5, 11mm
UNITED ORTHOPEDIC CORP.
2303-3052
In Commercial Distribution

  • 04712602348218 ()

  • 11mm
2303-3052

  • Posterior-stabilized total knee prosthesis
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 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 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
TELIX K Ti Cage 11x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1136
In Commercial Distribution

  • 04250869607810 ()
109-015-1136

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 10x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1036
In Commercial Distribution

  • 04250869607803 ()
109-015-1036

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 9x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-0936
In Commercial Distribution

  • 04250869607797 ()
109-015-0936

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 8x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-0836
In Commercial Distribution

  • 04250869607780 ()
109-015-0836

  • Metallic spinal interbody fusion cage
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