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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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Connector, Parallel, C-C, Large
Spine Wave, Inc.
11-7403
In Commercial Distribution

  • 10840642139921 ()
11-7403

  • Bone-screw internal spinal fixation system connector
Connector, Parallel, C-C, Medium
Spine Wave, Inc.
11-7402
In Commercial Distribution

  • 10840642139914 ()
11-7402

  • Bone-screw internal spinal fixation system connector
Connector, Parallel, C-C, Small
Spine Wave, Inc.
11-7401
In Commercial Distribution

  • 10840642139907 ()
11-7401

  • Bone-screw internal spinal fixation system connector
CC TOP OF CART
MEDLINE INDUSTRIES, INC.
ACC010253C
In Commercial Distribution

  • 10888277885950 ()
ACC010253C

  • General surgical procedure kit, non-medicated, reusable
CC MAGNESIUM 3750 Tests
ABBOTT IRELAND
03P6834
In Commercial Distribution

  • 00380740169862 ()
03P6834

  • Magnesium (Mg2+) IVD, kit, spectrophotometry
CC MAGNESIUM 1000 Tests
ABBOTT IRELAND
03P6824
In Commercial Distribution

  • 00380740169855 ()
03P6824

  • Magnesium (Mg2+) IVD, kit, spectrophotometry
CC CARTER TOTAL KNEE
MEDLINE INDUSTRIES, INC.
DYNJ904142L
In Commercial Distribution

  • 10193489365948 ()
DYNJ904142L

  • General surgical procedure kit, non-medicated, single-use
CC CARTER TOTAL KNEE
MEDLINE INDUSTRIES, INC.
DYNJ904142G
In Commercial Distribution

  • 10193489595710 ()
DYNJ904142G

  • General surgical procedure kit, non-medicated, single-use
CC CARTER TOTAL KNEE
MEDLINE INDUSTRIES, INC.
DYNJ904142I
In Commercial Distribution

  • 10193489661095 ()
DYNJ904142I

  • General surgical procedure kit, non-medicated, single-use
NATRELLE 133FX-13, 550 cc
Allergan, Inc.
133FX-13
Not in Commercial Distribution

  • 10888628004009 ()

  • 550 cc
133FX-13

  • Skin-port tissue expander
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