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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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PEGGED GLENOID TRIL & DRILL GUIDE CADDY
ARTHREX, INC.
AR-9225CP
In Commercial Distribution

  • 00888867137769 ()
AR-9225CP

  • Device sterilization/disinfection container, reusable
KEELED GLENOID TRIAL & DRILL GUIDE CADDY
ARTHREX, INC.
AR-9225CK
In Commercial Distribution

  • 00888867137752 ()
AR-9225CK

  • Device sterilization/disinfection container, reusable
GLENOID VERSION CORRECTION SYS INST CASE
ARTHREX, INC.
AR-9215C
In Commercial Distribution

  • 00888867137714 ()
AR-9215C

  • Device sterilization/disinfection container, reusable
KEEL GLENOID DRILL GUIDE # 2, X-LARGE
ARTHREX, INC.
AR-9215-9
Not in Commercial Distribution

  • 00888867137691 ()
AR-9215-9

  • Surgical drill guide, reusable
GLENOID DRILL GUIDE #1, X-LARGE
ARTHREX, INC.
AR-9215-8
Not in Commercial Distribution

  • 00888867137677 ()
AR-9215-8

  • Surgical drill guide, reusable
UNIVERS II CONGRUENT RMR INSTR CS
ARTHREX, INC.
AR-9200RRC
In Commercial Distribution

  • 00888867137097 ()
AR-9200RRC

  • Device sterilization/disinfection container, reusable
UNIVERS CA HUMERAL HEAD INSTRUMENT CASE
ARTHREX, INC.
AR-9200CAC
In Commercial Distribution

  • 00888867137073 ()
AR-9200CAC

  • Device sterilization/disinfection container, reusable
UNIVERS TRIAL STEM, 5MM
ARTHREX, INC.
AR-9200-15
In Commercial Distribution

  • 00888867136854 ()
AR-9200-15

  • Humeral stem prosthesis trial, reusable
HUMERAL RESECTION TEMPLATE, RIGHT
ARTHREX, INC.
AR-9200-01R
In Commercial Distribution

  • 00888867136830 ()
AR-9200-01R

  • Surgical implant template, reusable
HUMERAL RESECTION TEMPLATE, LEFT
ARTHREX, INC.
AR-9200-01L
In Commercial Distribution

  • 00888867136823 ()
AR-9200-01L

  • Surgical implant template, reusable
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