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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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CoRoent XL-H, 2x22x60mm 20°
Nuvasive, Inc.
6200260P2
In Commercial Distribution

  • 00887517680860 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-H, 2x22x55mm 20°
Nuvasive, Inc.
6200255P2
In Commercial Distribution

  • 00887517680853 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-H, 2x22x50mm 20°
Nuvasive, Inc.
6200250P2
In Commercial Distribution

  • 00887517680846 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-H, 2x22x45mm 20°
Nuvasive, Inc.
6200245P2
In Commercial Distribution

  • 00887517680839 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-H, 2x22x40mm 20°
Nuvasive, Inc.
6200240P2
In Commercial Distribution

  • 00887517680822 ()


  • Polymeric spinal interbody fusion cage
Brevia Catheter Kit, 20
Bard Access Systems, Inc.
5563200
Not in Commercial Distribution

  • 10801741045438 ()
  • 00801741045431 ()
  • 20801741045435 ()

  • Length: 20 Centimeter
  • Catheter Gauge: 11 French
5563200

  • Double-lumen haemodialysis catheter, implantable
BASE Trial 20° Set
Nuvasive, Inc.
BASETRIAL20
In Commercial Distribution

  • 00887517725363 ()


  • Device sterilization/disinfection container, reusable
Modulus ALIF, 12x42x32mm 20°
Nuvasive, Inc.
1921092P2
In Commercial Distribution

  • 00887517020659 ()


  • Metallic spinal interbody fusion cage
Modulus ALIF, 10x42x32mm 20°
Nuvasive, Inc.
1921091P2
In Commercial Distribution

  • 00887517020642 ()


  • Metallic spinal interbody fusion cage
Modulus ALIF, 8x42x32mm 20°
Nuvasive, Inc.
1921090P2
In Commercial Distribution

  • 00887517020635 ()


  • Metallic spinal interbody fusion cage
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