ULTRASOL OXY WIPES
Disinfection Wipe for surfaces
CE Class IIb oxidative-based disinfectant wipes for cleaning and disinfecting medical devices and medical inventory in areas with increased efficacy requirements. The wipes have a broad spectrum of activity against bacteria and viruses, including spores.
Special features
- MD IIb & BPR PT2, PT4
- A broad spectrum of activity against bacteria, viruses and spores
- A high level of material compatibility
- No toxic or environmentally harmful residues on the surface
- Wipe material: 40 % viscose & 60% PET
- Size of the wipe: 200 x 200 mm
The wipes have a broad spectrum of activity against bacteria and
viruses, including spores.
Thanks to its oxidative base, ULTRASOL OXY WIPES have a
high level of material compatibility and can be used on almost
all materials. It leaves no toxic or environmentally harmful
residues on the surface.
Wipe material: 40 % viscose & 60% PET
Size of the wipe: 200 x 200 mm
SPECTRUM OF ACTIVITY AND CONTACT TIMES:
• bactericidal & levurocidal 5 min
EN 13624 (clean and dirty conditions)
EN 13727 (clean and dirty conditions)
EN 16615 (clean and dirty conditions)
• tuberculocidal 5 min
EN 14348 (clean and dirty conditions)
• mycobactericidal 5 min
EN 14348 (clean and dirty conditions)
• sporicidal against C. diff. 5 min
EN 17126 (dirty conditions)
EN 17846 (dirty conditions)
• sporicidal 15 min
EN 17126 (clean and dirty conditions)
EN 17846 (clean and dirty conditions)
• fungicidal 5 min
EN 13624 (clean and dirty conditions)
• virucidal 5 min
EN 14476 (clean and dirty conditions)
• limited virucidal 5 min
EN 14476 (clean and dirty conditions)
Additional test results:
• bactericidal 1 min
EN 1276 (dirty conditions)
• yeasticidal (Candida albicans) 1 min
EN 1650 (dirty conditions)
• sporicidal 15 min
EN 13704 (dirty conditions)
The spectrum of activity and contact times apply both to use as a biocide and as a medical device.
Links
Materials
According to Biocidal Products Regulation (BPR):
For rapid disinfection and cleaning of alcohol sensitive medical equipment and surfaces of every type.
Acc. to EU Medical Devices Regulation:
Rapid disinfection and cleaning of non-invasive and invasive medical devices, especially for sensitive surfaces of medical devices.
Further areas of application:
In addition to the medical sector also suitable for the food sector and large canteen kitchens as well as for industry and public facilities.
NSF D2 - Certified (173370).
POLAND
| Package Size | Product Code | GTIN |
|---|---|---|
| 6 x 72 pcs | 01-270-T072FI | 4066625004645 |
+ 5 - +25 °C
1,5 years from manufacturing
Wipe surfaces with ULTRASOL OXY WIPES until completely wet. In routine use, the disinfected surfaces can be used again immediately after drying. If you are disinfecting transvaginal or transrectal ultrasound probes, or other Class IIb medical devices, rinse the surfaces after the required contact time. For the targeted disinfection of semicritical medical devices, the exposure time before reuse must be taken into account.
Use personal protective equipment (protective gloves).
Suitable for the disinfection of semicritical medical devices (e.g. probes). When using, please follow the instructions provided by the medical device manufacturer. When disinfecting incubators for premature
infants, the KRINKO guidelines must be observed.
According to the EU Medical Device Regulation, users/patients are obligated to report any serious incident that has occurred in relation to the device to the manufacturer and the competent authority of
the EU Member State in which the user/patient is established.
Shelf life after opening: 42 days.
| SPECTRUM OF ACTIVITY AND CONTACT TIMES * | 1 min | 5min | 15 min | ||
| Recommendation for surface disinfection | |||||
| bactericidal, levurocidal | EN 13624 EN 13727 EN 16615 | clean and dirty conditions | x | ||
| tuberculocidal | EN 14348 | clean and dirty conditions | x | ||
| mycobactericidal | EN 14348 | clean and dirty conditions | x | ||
| sporicidal against C. diff. | EN 17126 EN 17846 | dirty conditions | x | ||
| sporicidal | EN 17126 EN 17846 | clean and dirty conditions | x | ||
| fungicidal | EN 13624 | clean and dirty conditions | x | ||
| virucidal | EN 14476 | clean and dirty conditions | x | ||
| limited virucidal | EN 14476 | clean and dirty conditions | x | ||
| Additional test results | |||||
| bactericidal | EN 1276 | dirty conditions | x | ||
| yeasticidal (Candida albicans) | EN 1650 | dirty conditions | x | ||
| sporicidal | EN 13704 | dirty conditions | x | ||
| * The spectrum of activity and contact times apply both to use as a biocide and as a medical device. | |||||
According to the EU Medical Device Regulation, users/patients are obligated to report any serious incident that has occurred in relation to the device to the manufacturer and the competent authority of
the EU Member State in which the user/patient is established.
Use disinfectants safely. Always read label, product information and safety data sheet before use.
Read the usage and security instructions from the safety data sheet.
Hydrogen Peroxide 7g
Peracetic Acid 0,1g
Glycolic Acid 0,1g
