ΜEDABUR

Ready-to-use disinfectant for rotary instruments and burs

ΜΕDABUR is a ready-to-use detergent disinfectant specially designed to clean and disinfect dental micro-instruments. It effectively removes organic soil such as blood, saliva, etc. and has excellent disinfection properties.
It has been specially formulated for rotary endodontic instruments such as burs, diamonds, polishers, etc.
Its formulation prevents instrument corrosion and discoloration even in prolonged immersion.
MEDABUR is free of aldehydes, phenols, chlorine and EDTA.

Properties

  • Ready-to-use solution
  • Drastically removes organic residues
  • Use in immersion bath or ultrasonic bath
  • Prevents corrosion and instrument discoloration
  • Bactericidal, yeasticidal, tuberculocidal, mycobactericidal
  • Virucidal (HBV, HIV, HCV, Herpes, Vaccinia, BVDV, Vaccinia,
    Influenza, Εbola, Coronavirus)

Microbiological efficacy

MEDABUR - Microbiological efficacy

  1. DVV: Deutsche Vereinigung zur Bekämpfung der Viruskrankheiten / German Association for the Control of Virus Diseases
  2. RKI: Robert Koch Institute – German Federal Health Authority

Ultrasonic bath

MEDABUR can be used in all common types of ultrasonic baths

MEDABUR - Ready-to-use disinfectant for rotary instruments and burs

Packaging

  • 2.5 litre bottle (Ref. 20005)

Physical properties

  • Appearance: Light blue solution
  • Density: 0.99 g/cm3 at 20˚C
  • pH: 9.5-11.0 at 20˚C
  • Odour: Neutral
  • Storage: 5˚C – 35˚C
  • Stability: 3 Years
  • Biodegradability: According to OCDE 301D

Compatibility

MEDABUR is compatible with most materials such as stainless steel, aluminium, glass, ceramics, hard plastics, ebonite, etc … MEDABUR is not compatible with disinfecting preparations containing aldehydes.

Composition

N- (3-aminopropyl) -N dodecylpropano-1,3-diamine, non ionic surfactants <5%, isopropanol, corrosion inhibitor, anti-foaming agent, excipients.

MEDABUR is manufactured in the EU. MEDALKAN satisfies the requirements of ISO 9001:2015 for quality management system and the requirements of ISO 13485:2016 for the design and manufacture of medical devices.

ISO 9001, ISO 13485, CE
  • CE mark according to the medical devices Directive
    (Directive 93/42/EEC)
  • Medical device class IIb