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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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TLIF CURVED TRIAL L28 x W9 x A8 x H13
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039820646 ()
TC.2117

  • Spinal fixation plate, non-bioabsorbable
TLIF CURVED TRIAL L28 x W9 x A8 x H12
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039820639 ()
TC.2116

  • Spinal fixation plate, non-bioabsorbable
TLIF CURVED TRIAL L28 x W9 x A8 x H11
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039820622 ()
TC.2115

  • Spinal fixation plate, non-bioabsorbable
TLIF CURVED TRIAL L28 x W9 x A8 x H10
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039820615 ()
TC.2114

  • Spinal fixation plate, non-bioabsorbable
TLIF CURVED TRIAL L28 x W9 x A8 x H9
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039820608 ()
TC.2113

  • Spinal fixation plate, non-bioabsorbable
TLIF CURVED TRIAL L28 x W9 x A8 x H8
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039820592 ()
TC.2112

  • Spinal fixation plate, non-bioabsorbable
Interbody Fusion Device 7DEG x 26L x 10W x 9H
CAMBER SPINE TECHNOLOGIES, LLC
CX-261009
In Commercial Distribution

  • B030CX2610090 ()
CX-261009

  • Polymeric spinal interbody fusion cage
Interbody Fusion Device 7DEG x 22L x 10W x 15H
CAMBER SPINE TECHNOLOGIES, LLC
CK-221015
In Commercial Distribution

  • B030CK2210150 ()


  • Polymeric spinal interbody fusion cage
Interbody Fusion Device 7DEG x 22L x 10W x 14H
CAMBER SPINE TECHNOLOGIES, LLC
CK-221014
In Commercial Distribution

  • B030CK2210140 ()


  • Polymeric spinal interbody fusion cage
Interbody Fusion Device 7DEG x 22L x 10W x 13H
CAMBER SPINE TECHNOLOGIES, LLC
CK-221013
In Commercial Distribution

  • B030CK2210130 ()


  • Polymeric spinal interbody fusion cage
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