The ë WRAP sterilization wrap, designed for tools and cassettes, is splash-resistant. Filtering, machine washable and dryable up to 75 times*, it can also be sterilized up to 75 cycles at a maximum temperature of 134°C, following your sterilizer/autoclave’s usual procedures.
The ë WRAP sterilization wraps are made using ReSteri technology and tested in independent ISO 17025-certified laboratories, in compliance with CAN/CSA Z314:23, EN 868 and ISO 11607-2:2019 standards. Custom sizes can also be manufactured (minimum quantity required).
Contact us for a custom order
Price range from
$24,00$ to $47,50$
(volume discount)
| Size | Inches | Centimeters |
|---|---|---|
| XS | 13'' × 13'' | 33 × 33 cm |
| S | 16'' × 16'' | 40.5 × 40.5 cm |
| M | 20'' × 20'' | 50.5 × 50.5 cm |
| L | 24'' × 24'' | 61 × 61 cm |
| XL | 30'' × 30'' | 76 × 76 cm |
Composition and sizes available
How to use the ë WRAP
Easy wash cycles
Step 1: Place used items in a mesh laundry bag.
Step 2: Machine wash. Hot water between 50 and 71°C with neutral detergent, no additives, 30-minute cycle (other disinfection methods are possible, contact us).
Step 3: Tumble dry on high heat between 50 and 90°C.
Step 4: Mark with an indelible (permanent) pen or scan with your smartphone to track the number of completed cycles.
Step 5: Store for next use. Flat, folded, nose wires straightened, wash your hands and clean surfaces before handling.
Note:
ë WRAP sterilization wrap instructions click here (FR)
Products are developed using the ëncore technology and ReSteri™ technology recipes and are reusable up to 100 times (ëncore products) / 75 times (ReSteri™ products).* Zero waste and circular, all components are recyclable or recovered to become pellets or fibers.
* Follow care instructions.
Certifications and compliance
- CSA Z314:F23 Reprocessing of medical devices in Canada in all health care settings
- ISO 11607-1:2019 ackaging for terminally sterilized medical devices / Part 1: Requirements for materials, sterile barrier systems and packaging systems
- EN 868 Packaging for medical devices to be sterilized
- ISO 11607-2:2019 Packaging for terminally sterilized medical devices / Part 2: Validation requirements for forming, sealing and assembly processes
- Processing of reusable surgical textiles for use in health care facilities
- ANSI/AAMI ST67:2011 (R2017) Sterilization of health care products — Requirements and guidance for selecting a sterility assurance level (SAL) for products labeled "sterile"
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