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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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UNIVERSAL BLOCK PACK 6 5
Cardinal Health 200, LLC
34A5660A
In Commercial Distribution

  • 50197106081981 ()
  • 10197106081983 ()
34A5660A

  • Intrathecal anaesthesia set, non-medicated
JOURNEY CHAMFER BLOCK - SIZE 5
Smith & Nephew, Inc.
E0017471-4
In Commercial Distribution

  • 00885556813874 ()
E0017471-4

  • Orthopaedic prosthesis implantation positioning instrument, reusable
GLENOID SIZER 5 DEG L
Smith & Nephew, Inc.
SZR-0990-815-305
In Commercial Distribution

  • 00885556812204 ()
SZR-0990-815-305

  • Shoulder glenoid fossa prosthesis trial
GLENOID SIZER 5 DEG M
Smith & Nephew, Inc.
SZR-0990-815-205
In Commercial Distribution

  • 00885556812181 ()
SZR-0990-815-205

  • Shoulder glenoid fossa prosthesis trial
GLENOID SIZER 5 DEG S
Smith & Nephew, Inc.
SZR-0990-815-105
In Commercial Distribution

  • 00885556812167 ()
SZR-0990-815-105

  • Shoulder glenoid fossa prosthesis trial
GLENOID SIZER 5 DEG XS
Smith & Nephew, Inc.
SZR-0990-815-005
In Commercial Distribution

  • 00885556812143 ()
SZR-0990-815-005

  • Shoulder glenoid fossa prosthesis trial
CoRoent LO Titanium, 9x10x40 5°
Nuvasive, Inc.
6080940P
In Commercial Distribution

  • 00887517032492 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Titanium, 9x10x35 5°
Nuvasive, Inc.
6080935P
In Commercial Distribution

  • 00887517032485 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Titanium, 9x10x30 5°
Nuvasive, Inc.
6080930P
In Commercial Distribution

  • 00887517032478 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Titanium, 14x10x40 5°
Nuvasive, Inc.
6081440P
In Commercial Distribution

  • 00887517046093 ()


  • Metallic spinal interbody fusion cage
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