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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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CASE 9182050 ENDPLTE PREP ROUGEUR OUTER
MEDTRONIC SOFAMOR DANEK, INC.
9182050
In Commercial Distribution

  • 00613994185082 ()


  • Instrument tray, reusable
CASE X0406070 SPEC CROSSLINK INST TRAY
MEDTRONIC SOFAMOR DANEK, INC.
X0406070
Not in Commercial Distribution

  • 00613994177094 ()


  • Instrument tray, reusable
CASE 8690001 COBALT CHROME ROD MODULE
MEDTRONIC SOFAMOR DANEK, INC.
8690001
In Commercial Distribution

  • 00613994161574 ()


  • Instrument tray, reusable
Bear Chart SET with Carrying case
RIGHT MFG. CO., LTD.
Retinomax K+Screeen
Not in Commercial Distribution

  • 04562230698854 ()
RDA1172BA

  • Automated ophthalmic refractometer
Fireworks Chart SET with Carrying case
RIGHT MFG. CO., LTD.
Retinomax K+Screeen
Not in Commercial Distribution

  • 04562230698809 ()
RDA1182BA

  • Automated ophthalmic refractometer
Tulip Chart SET with Carrying case
RIGHT MFG. CO., LTD.
Retinomax K+Screeen
Not in Commercial Distribution

  • 04562230698755 ()
RDA1152BA

  • Automated ophthalmic refractometer
Bear Chart SET with Carrying case
RIGHT MFG. CO., LTD.
Retinomax Screeen
Not in Commercial Distribution

  • 04562230698700 ()
RDA1132BA

  • Automated ophthalmic refractometer
Fireworks Chart SET with Carrying case
RIGHT MFG. CO., LTD.
Retinomax Screeen
Not in Commercial Distribution

  • 04562230698656 ()
RDA1142BA

  • Automated ophthalmic refractometer
Tulip Chart SET with Carrying case
RIGHT MFG. CO., LTD.
Retinomax Screeen
Not in Commercial Distribution

  • 04562230698601 ()
RDA1112BA

  • Automated ophthalmic refractometer
LID 7574000L INSTR CASE LID TRIPLE
MEDTRONIC SOFAMOR DANEK, INC.
7574000L
In Commercial Distribution

  • 00613994325396 ()


  • Instrument tray, reusable
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