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Applied Medical Technology ST9000 - Remora Smoke and Fluid Tube Evacuator, Standard Size, 10/BX

Applied Medical Technology # ST9000 - Remora Smoke and Fluid Tube Evacuator, Standard Size, 10/BX
Part Number Applied Medical Technology ST9000
SKU Number CIA8009150
Sell Unit BOX
Ships Within Call for Availability
List Price $270.14
Product Description

Applied Medical Technology ST9000 - Remora Smoke and Fluid Tube Evacuator, Standard Size, 10/BX

Remora - Smoke and Fluid Tube Evacuator

Remora Smoke and fluids are removed at the origin of electrosurgical tip for a healthier environment.

The Remora allows the surgeon to simultaneously remove electrosurgical smoke and fluid from the surgical site. With a minimalist form, the Remora preserves the surgeons field of vision and control while operating. Additionally, the removal of fluid from the area can improve the conductivity of electrosurgical instruments, which may result in a more efficient procedure. The Remora comes in a variety of sizes to accommodate many different tips (blade, extended, or needle) and electrosurgical pencil handles. The Remora is an excellent tool to increase efficiency and assist in keeping the operating room free of toxic smoke.

  • All kits come with evacuator and needle tip adapter
  • Electrocautery unit not included.
  • QTY/Box 10 ea

Soft Material


  • Improved safety as carcinogens and other toxins are removed from the OR
  • Simultaneous smoke and fluid removal
  • Instantaneous removal at point of origin
  • Improved visibility
  • Compliant material protects delicate tissues
  • Unimpeded maneuverability
  • Insulates the pencil tip
  • Alternate ports prevent blockage and reduce trauma to tissue
  • OSHA and AORN smoke evacuation compliant
NOTE: The Needle Tip Adapter should not extend greater than 3mm past the suction port for optimal smoke and luid removal.


All Remora Evacuators are for use with either blade or needle electrodes.

The universal rear adapter connects to any filtered operating room vacuum source.

Device Characteristics

What MRI safety information does the labeling contain?Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):No
Device labeled as "Not made with natural rubber latex":Yes
For Single-Use:Yes
Prescription Use (Rx):Yes
Over the Counter (OTC):No
Kit:No
Combination Product:No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):No
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