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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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Trial Liner 20° 32/60-70 (E)
ORTHOMEDFLEX LLC
112152523
In Commercial Distribution

  • M7161121525230 ()
112-152-523

  • Acetabulum prosthesis trial, prefabricated, reusable
Trial Liner 20° 32/56-58 (D)
ORTHOMEDFLEX LLC
112152522
In Commercial Distribution

  • M7161121525220 ()
112-152-522

  • Acetabulum prosthesis trial, prefabricated, reusable
Trial Liner 20° 32/52-54 (C)
ORTHOMEDFLEX LLC
112152521
In Commercial Distribution

  • M7161121525210 ()
112-152-521

  • Acetabulum prosthesis trial, prefabricated, reusable
Trial Liner 20° 32/48-50 (B)
ORTHOMEDFLEX LLC
112152520
In Commercial Distribution

  • M7161121525200 ()
112-152-520

  • Acetabulum prosthesis trial, prefabricated, reusable
Trial Liner 20° 28/52-54 (C)
ORTHOMEDFLEX LLC
112152519
In Commercial Distribution

  • M7161121525190 ()
112-152-519

  • Acetabulum prosthesis trial, prefabricated, reusable
Trial Liner 20° 28/48-50 (B)
ORTHOMEDFLEX LLC
112152518
In Commercial Distribution

  • M7161121525180 ()
112-152-518

  • Acetabulum prosthesis trial, prefabricated, reusable
Trial Liner 20° 28/44-46 (A)
ORTHOMEDFLEX LLC
112152517
In Commercial Distribution

  • M7161121525170 ()
112-152-517

  • Acetabulum prosthesis trial, prefabricated, reusable
INSTRUMENT 3280041 RASP 12X20 20 DEG
MEDTRONIC SOFAMOR DANEK, INC.
3280041
In Commercial Distribution

  • 00721902798450 ()


  • Bone file/rasp, manual, reusable
CORTICAL SHANK, Cannulated, 9.5 X 20
Seaspine Orthopedics Corporation
MC1-195020
Not in Commercial Distribution

  • 10889987169583 ()
MC1-195020

  • Spinal bone screw, non-bioabsorbable
CORTICAL SHANK, Cannulated, 9.0 X 20
Seaspine Orthopedics Corporation
MC1-190020
Not in Commercial Distribution

  • 10889987169392 ()
MC1-190020

  • Bone-screw internal spinal fixation system, non-sterile
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