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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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Low Density 14mm x 16mm x 7° x 8mm
AURORA SPINE, INC.
116-14167-08-LD
In Commercial Distribution

  • B5211161416708LD0 ()


  • Metallic spinal interbody fusion cage
High Density 14mm x 16mm x 7° x 8mm
AURORA SPINE, INC.
116-14167-08-HD
In Commercial Distribution

  • B5211161416708HD0 ()


  • Metallic spinal interbody fusion cage
Mid Density 14mm x 16mm x 7° x 7mm
AURORA SPINE, INC.
116-14167-07-MD
In Commercial Distribution

  • B5211161416707MD0 ()


  • Metallic spinal interbody fusion cage
Low Density 14mm x 16mm x 7° x 7mm
AURORA SPINE, INC.
116-14167-07-LD
In Commercial Distribution

  • B5211161416707LD0 ()


  • Metallic spinal interbody fusion cage
High Density 14mm x 16mm x 7° x 7mm
AURORA SPINE, INC.
116-14167-07-HD
In Commercial Distribution

  • B5211161416707HD0 ()


  • Metallic spinal interbody fusion cage
Mid Density 14mm x 16mm x 7° x 6mm
AURORA SPINE, INC.
116-14167-06-MD
In Commercial Distribution

  • B5211161416706MD0 ()


  • Metallic spinal interbody fusion cage
Low Density 14mm x 16mm x 7° x 6mm
AURORA SPINE, INC.
116-14167-06-LD
In Commercial Distribution

  • B5211161416706LD0 ()


  • Metallic spinal interbody fusion cage
High Density 14mm x 16mm x 7° x 6mm
AURORA SPINE, INC.
116-14167-06-HD
In Commercial Distribution

  • B5211161416706HD0 ()


  • Metallic spinal interbody fusion cage
Mid Density 14mm x 16mm x 7° x 5mm
AURORA SPINE, INC.
116-14167-05-MD
In Commercial Distribution

  • B5211161416705MD0 ()


  • Metallic spinal interbody fusion cage
Low Density 14mm x 16mm x 7° x 5mm
AURORA SPINE, INC.
116-14167-05-LD
In Commercial Distribution

  • B5211161416705LD0 ()


  • Metallic spinal interbody fusion cage
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