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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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ATLANTIS Abutment Zr 20
DENTSPLY IH, INC.
35513
In Commercial Distribution

  • 07392532177255 ()


  • Transgingival implant
20° UniAbutment Pick-up - 4.3
Dentsply Implants Manufacturing GmbH
22882
In Commercial Distribution

  • 07392532037221 ()
22882

  • Dental implant suprastructure, temporary, preformed, reusable
20° UniAbutment Pick-up - 5.5
Dentsply Implants Manufacturing GmbH
22876
In Commercial Distribution

  • 07392532037160 ()
22876

  • Dental implant suprastructure, temporary, preformed, reusable
BASE Trial 20° Set
Nuvasive, Inc.
BASETRIAL20
In Commercial Distribution

  • 00887517725363 ()


  • Device sterilization/disinfection container, reusable
Brigade Hyperlordotic, 14x42x32mm 20°
Nuvasive, Inc.
7502144
In Commercial Distribution

  • 00887517420152 ()


  • Polymeric spinal interbody fusion cage
Brigade Hyperlordotic, 12x42x32mm 20°
Nuvasive, Inc.
7502142
In Commercial Distribution

  • 00887517420145 ()


  • Polymeric spinal interbody fusion cage
Brigade Hyperlordotic, 10x42x32mm 20°
Nuvasive, Inc.
7502140
In Commercial Distribution

  • 00887517420138 ()


  • Polymeric spinal interbody fusion cage
Brigade Hyperlordotic, 8x42x32mm 20°
Nuvasive, Inc.
7502138
In Commercial Distribution

  • 00887517420121 ()


  • Polymeric spinal interbody fusion cage
Brigade Hyperlordotic, 6x42x32mm 20°
Nuvasive, Inc.
7502136
In Commercial Distribution

  • 00887517420114 ()


  • Polymeric spinal interbody fusion cage
Brigade Hyperlordotic, 14x42x30mm 20°
Nuvasive, Inc.
7502135
In Commercial Distribution

  • 00887517420107 ()


  • Polymeric spinal interbody fusion cage
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