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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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BEQ-HMOD 70000-USA Adult Quadrox iD, Softshell Venous Reser. 800ml, Better Bladder 1/4, BEQ-RF32 RotaFlow, Blood Microfilter System SQ 40 S, Prebypass filter w/o Vent Porous Media 3/8x3/8, Gas Filter
DATASCOPE CORP.
BEQ-TOP 8102
Not in Commercial Distribution

  • 00607567201101 ()
701049526

  • Cardiopulmonary bypass system blood tubing set
No Description
BESMED HEALTH BUSINESS CORP.
RE-21345
In Commercial Distribution

  • 04716770213453 ()


  • PEEP valve, reusable
No Description
BESMED HEALTH BUSINESS CORP.
RE-21340
In Commercial Distribution

  • 04716770213408 ()


  • PEEP valve, reusable
No Description
BESMED HEALTH BUSINESS CORP.
RE-21335
In Commercial Distribution

  • 04716770213354 ()


  • PEEP valve, reusable
No Description
BESMED HEALTH BUSINESS CORP.
RE-21330
In Commercial Distribution

  • 04716770213309 ()


  • PEEP valve, reusable
No Description
BESMED HEALTH BUSINESS CORP.
RE-21320
In Commercial Distribution

  • 04716770213200 ()


  • PEEP valve, single-use
No Description
FLEXICARE MEDICAL LIMITED
038-965-030U
In Commercial Distribution

  • 05055788730354 ()


  • Reinforced endotracheal tube, single-use
No Description
FLEXICARE MEDICAL LIMITED
038-965-035U
In Commercial Distribution

  • 05055788730316 ()


  • Reinforced endotracheal tube, single-use
No Description
FLEXICARE MEDICAL LIMITED
038-965-040U
In Commercial Distribution

  • 05055788730279 ()


  • Reinforced endotracheal tube, single-use
No Description
FLEXICARE MEDICAL LIMITED
038-965-065U
In Commercial Distribution

  • 05055788730040 ()


  • Reinforced endotracheal tube, single-use
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