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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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20 GA PNEUMATIC HSV CUTTER
Bausch & Lomb Incorporated
CX6802
In Commercial Distribution

  • 20757770482614 ()
  • 00757770482610 ()
CX6802

  • Vitrectomy system micro-cutting unit
MILL LASER ENDOPROBE 20 ANGLED
Bausch & Lomb Incorporated
CX5981
In Commercial Distribution

  • 20757770469943 ()
  • 00757770469949 ()
CX5981

  • Phacoemulsification/vitrectomy system
MILL LASER ENDOPROBE 20 TAPER
Bausch & Lomb Incorporated
CX5980
In Commercial Distribution

  • 20757770469936 ()
  • 00757770469932 ()
CX5980

  • Phacoemulsification/vitrectomy system
TLX Trial, 7-14mm 20° Expandable
Nuvasive, Inc.
1780200
In Commercial Distribution

  • 00887517936103 ()


  • Surgical implant/trial-implant/sizer holder, reusable
Beamsplitter Coupler, C-Mount, 20 mm
STRYKER CORPORATION
1088020120
Not in Commercial Distribution

  • 07613327054651 ()
1088-020-120

  • Endoscope camera adaptor
BI-OK Steam Vials (20/pack)
PROPPER MANUFACTURING COMPANY, INC.
26920000
In Commercial Distribution

  • 30818087012332 ()
  • 10818087012338 ()


  • Biological sterilization indicator
Interlock II Ti-C, 16x19x16mm 20°
Nuvasive, Inc.
6779620CP2
In Commercial Distribution

  • 00887517813664 ()


  • Polymeric spinal interbody fusion cage
Interlock II Ti-C, 14x19x16mm 20°
Nuvasive, Inc.
6779420CP2
In Commercial Distribution

  • 00887517813541 ()


  • Polymeric spinal interbody fusion cage
Interlock II Ti-C, 13x19x16mm 20°
Nuvasive, Inc.
6779320CP2
In Commercial Distribution

  • 00887517813480 ()


  • Polymeric spinal interbody fusion cage
Interlock II Ti-C, 14x17x14mm 20°
Nuvasive, Inc.
6771420CP2
In Commercial Distribution

  • 00887517812780 ()


  • Polymeric spinal interbody fusion cage
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