NOSOCLEAR

Rinse aid for the automated reprocessing of surgical instruments and equipment

NOSOCLEAR is a very concentrated rinse aid especially formulated for the fast and spotless drying of surgical instruments, glassware, and other sensitive medical devices.

It can be used on stainless steel instruments, ophthalmological instruments, anesthetic equipment, laboratory glassware, plastics and hard rubbers.

NOSOCLEAR reduces the surface tension of the water on the instruments allowing them to dry quickly without leaving any traces.

NOSOCLEAR can be used in automatic washers, washer-disinfectors, cart and tunnel washers or other instrument reprocessing equipment.

Properties

  • Drastically shortens drying time
  • Leaves the instruments filmless and spotfree
  • Very economical: 0,01% to 0,03% dilution
  • Can be used in soft or hard water
  • Does not foam, prevents corrosion and instruments
    discoloration
  • Appropriate for heat-resistant as well as heat-sensitive
    instruments

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.

NOSOCLEAR - Rinse aid for the automated reprocessing of surgical instruments and equipment

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: <50 mPas at 20˚C
  • Storage: 5˚C – 35˚C
  • Stability: 3 Years
  • Biodegradability: According to OCDE 301D

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 Certification
CE-LOGO

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