SEARCH RESULTS FOR: (*Sandwhich Panel Machine*)(8646 results)

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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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BARCO - 00885556541098

FLAT PANEL LCD 26
Smith & Nephew, Inc.
72202591
In Commercial Distribution

  • 00885556541098 ()
72202591

  • Image display unit, colour

DeRoyal - 00749756569712

ULTRALIGN + TLSO POSTERIOR PANEL
DEROYAL INDUSTRIES, INC.
UPP2302
In Commercial Distribution

  • 00749756569712 ()
UPP2302

  • Lumbar spine orthosis

DeRoyal - 00749756569705

ULTRALIGN + TLSO POSTERIOR PANEL
DEROYAL INDUSTRIES, INC.
UPP2701
In Commercial Distribution

  • 00749756569705 ()
UPP2701

  • Lumbar spine orthosis

DeRoyal - 00749756569699

ULTRALIGN + TLSO POSTERIOR PANEL
DEROYAL INDUSTRIES, INC.
UPP2601
In Commercial Distribution

  • 00749756569699 ()
UPP2601

  • Lumbar spine orthosis

DeRoyal - 00749756569668

ULTRALIGN + TLSO POSTERIOR PANEL
DEROYAL INDUSTRIES, INC.
UPP2401
In Commercial Distribution

  • 00749756569668 ()
UPP2401

  • Lumbar spine orthosis

DeRoyal - 00749756569651

ULTRALIGN + TLSO POSTERIOR PANEL
DEROYAL INDUSTRIES, INC.
UPP2301
In Commercial Distribution

  • 00749756569651 ()
UPP2301

  • Lumbar spine orthosis

DeRoyal - 00749756569606

ULTRALIGN + LSO POSTERIOR PANEL
DEROYAL INDUSTRIES, INC.
UPP1402
In Commercial Distribution

  • 00749756569606 ()
UPP1402

  • Lumbar spine orthosis

DeRoyal - 00749756569590

ULTRALIGN + LSO POSTERIOR PANEL
DEROYAL INDUSTRIES, INC.
UPP1302
In Commercial Distribution

  • 00749756569590 ()
UPP1302

  • Lumbar spine orthosis

LEGION - 00885556613511

LEGION FEMORALTRIAL PANEL 7-8
Smith & Nephew, Inc.
71442167
In Commercial Distribution

  • 00885556613511 ()
71442167

  • Instrument tray, reusable

Sensititre GP Panel PLATE DRY CLI GRAM+ ID AUTO - 00848838074363

PLATE DRY CLI GRAM+ ID AUTO A semi-quantitative test intended for the automated identification of Gram positive bacterial isolates based on biochemical reactions. Used in a diagnostic workflow to aid clinicians in determining potential treatment options for patients suspected of having a microbial infection, the device requires an automated system to produce a result and requires a pure, agar grown culture. This device is for professional use only and is not a companion diagnostic.
REMEL, INC.
GPID
In Commercial Distribution

  • 00848838074363 ()


  • Multiple aerobic gram positive bacteria species culture isolate identification IVD, kit
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