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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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COHERE ALIF Interbody, 6x34x24mm 20°
Nuvasive, Inc.
1964420P2
In Commercial Distribution

  • 00195377067395 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 6x42x32mm 20°
Nuvasive, Inc.
1962020P2
In Commercial Distribution

  • 00195377067340 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 12x38x28mm 20°
Nuvasive, Inc.
1928820P2
In Commercial Distribution

  • 00195377067296 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 12x34x24mm 20°
Nuvasive, Inc.
1924420P2
In Commercial Distribution

  • 00195377067241 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 12x42x32mm 20°
Nuvasive, Inc.
1922020P2
In Commercial Distribution

  • 00195377067197 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 10x38x28mm 20°
Nuvasive, Inc.
1908820P2
In Commercial Distribution

  • 00195377067128 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 10x26x22mm 20°
Nuvasive, Inc.
1906220P2
In Commercial Distribution

  • 00195377067098 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 10x34x24mm 20°
Nuvasive, Inc.
1904420P2
In Commercial Distribution

  • 00195377067043 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 10x42x32mm 20°
Nuvasive, Inc.
1902020P2
In Commercial Distribution

  • 00195377067012 ()


  • Polymeric spinal interbody fusion cage
M-Core R-Li 20 Deep Brown
Ws Audiology Usa, Inc.
M-Core R-Li 20
In Commercial Distribution

  • 04056839053096 ()
10986198

  • Air-conduction hearing aid, receiver-in-canal
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