LaForce/Shambaugh replacement adenotome blade medium size 16.0mm wide

  • Replacement adenotome blade identified for LaForce/Shambaugh instrument applications.
  • Medium-size design provides a 16.0 mm blade width.
  • Specified blade width is 16.0 mm for this medium size.
  • Product is a replacement blade rather than a complete instrument.
  • Designed as an adenotome blade for LaForce/Shambaugh replacements.
  • The product description identifies this item as medium size.

Brand: surgivalley

$44.52 $56.00

(Verfügbar)
Menge
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SKU: 083030040

Kategorien: Adenotome

Tags: Adenotomes

LaForce/Shambaugh Replacement Adenotome Blade, Medium, 16.0 mm Wide

The LaForce/Shambaugh replacement adenotome blade is designed for compatible adenotome instruments used in ENT procedures. This medium-size blade measures 16.0 mm wide, providing a defined cutting profile for adenectomy and related soft-tissue applications. It is intended as a replacement component for facilities that maintain compatible LaForce or Shambaugh equipment, helping support instrument readiness and efficient operating room workflows. Before use, confirm instrument compatibility, inspect the blade for damage or wear, and follow your facility’s validated cleaning, sterilization, and handling procedures.

  • Replacement for compatible LaForce adenotome instruments
  • Replacement for compatible Shambaugh adenotome instruments
  • Adenectomy and related ENT soft-tissue procedures
  • Instrument set maintenance in hospitals, ASCs, and specialty clinics
Product typeReplacement adenotome blade
Compatible instrument brandsLaForce and Shambaugh
SizeMedium
Blade width16.0 mm
Quality AssuranceBoil Test: Passed
  • Inspect the blade and compatible instrument before each use; remove damaged or worn components from service.
  • Clean, sterilize, and store according to the instrument manufacturer’s instructions and your facility’s validated protocols.
  • Protect the cutting edge during handling and storage to help prevent damage.

Confirm compatibility and applicable processing requirements with your facility’s clinical engineering or sterile processing team before use.


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