NOSOCLEAR

Rinse aid for the automated reprocessing
of surgical instruments

NOSOCLEAR is a highly concentrated rinse aid specifically formulated for fast, spot-free drying of surgical instruments, laboratory glassware and other sensitive medical devices in automated reprocessing systems.

NOSOCLEAR reduces the surface tension of water on instrument surfaces, promoting rapid sheeting and efficient drying without leaving residues or water spots.

It is intended for use in washer-disinfectors, cart washers, tunnel washers, and other automated instrument reprocessing equipment.

NOSOCLEAR is compatible with stainless steel instruments, ophthalmological instruments, anesthetic equipment, laboratory glassware, plastics and hard rubbers.

Properties

  • Drastically shortens drying time
  • Leaves the instruments filmless and spotfree
  • Optimized for final rinse in washer-disinfectors
  • Very economical: 0,01% to 0,03% dilution
  • Effective in soft and hard water
  • Non-foaming formulation for automated systems
  • Prevents corrosion and instrument discoloration

Compatibility

NOSOCLEAR is compatible with most materials such as stainless steel, aluminum, glass, ceramics, hard plastics, ebonite, etc …
Material compatibility with sensitive materials should always be checked before use.

Composition

Non ionic surfactants 15% – 20%, phosphonates, corrosion inhibitor, pH regulator, excipients.

Rinse aid for the automated reprocessing of surgical instruments - NOSOCLEAR

Packaging

  • 5 litre canister (Ref. 20030)
  • 10 litre canister (Ref. 20031)

Physical properties

  • Appearance: Transparent yellow solution
  • Density: 1.02 g/cm3 at 20˚C
  • pH: 6.0 – 7.0 at 20˚C
  • pH (0.2 – 0.8 ml/l.): 7.0 – 8.0 (neutral) at 20˚C
  • Viscosity: Inferior to 50 mPas at 20˚C
  • Storage: 5˚C – 35˚C
  • Stability: 3 Years
  • Biodegradability: According to OCDE 301D

Downloads

ΝΟSOCLEAR – Product Data sheet (PDS)

NOSOCLEAR – Material safety data sheet (MSDS)

NOSOCLEAR is manufactured in the EU.
MEDALKAN satisfies the requirements of ISO 9001 for quality management system and the requirements of ISO 13485 for the design and manufacture of medical devices.

ISO and CE mark Certifications - MEDALKAN

  • CE mark according to the medical devices MDR Regulation (EU) 2017/745
  • Medical device class I