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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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SureMAX-SA — 10° Extra–Large 12
ADDITIVE IMPLANTS, LLC
1
In Commercial Distribution

  • 00817662025346 ()
1022-10152012

  • Metallic spinal interbody fusion cage
SureMAX-SA — 10° Extra–Large 11
ADDITIVE IMPLANTS, LLC
1
In Commercial Distribution

  • 00817662025339 ()
1022-10152011

  • Metallic spinal interbody fusion cage
SureMAX-SA — 10° Extra–Large 9
ADDITIVE IMPLANTS, LLC
1
In Commercial Distribution

  • 00817662025315 ()
1022-10152009

  • Metallic spinal interbody fusion cage
SureMAX-SA — 10° Extra–Large 8
ADDITIVE IMPLANTS, LLC
1
In Commercial Distribution

  • 00817662025308 ()
1022-10152008

  • Metallic spinal interbody fusion cage
SureMAX-SA — 10° Extra–Large 7
ADDITIVE IMPLANTS, LLC
1
In Commercial Distribution

  • 00817662025292 ()
1022-10152007

  • Metallic spinal interbody fusion cage
SureMAX-SA — 10° Extra–Large 6
ADDITIVE IMPLANTS, LLC
1
In Commercial Distribution

  • 00817662025285 ()
1022-10152006

  • Metallic spinal interbody fusion cage
Reflect Certus 5.0 X 10
INTEGRATED DENTAL SYSTEMS, LLC
RC5010C
In Commercial Distribution

  • 00817773022128 ()
RC5010C

  • Dental bone matrix implant, metallic
Reflect Certus 4.1 X 10
INTEGRATED DENTAL SYSTEMS, LLC
RC4110C
In Commercial Distribution

  • 00817773022074 ()
RC4110C

  • Dental bone matrix implant, metallic
Blade Electrode Non-Stick (10/PK)
Gyrus ACMI, LLC
568605
In Commercial Distribution

  • 00821925008458 ()


  • Electrosurgical return electrode, single-use
SLR-PLUS REVISION STEM 10 NON-CEMENTED
Smith & Nephew, Inc.
75002813
In Commercial Distribution

  • 07611996088229 ()
75002813

  • Press-fit femoral stem prosthesis
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