Frequently asked questions
Answers to the most common questions about U.Jet products, sterilization, certifications and orders.
Are your products sterile, and by which method?
Most U.Jet devices are single-use sterile, sterilized with ethylene oxide (EO). The sterility status and method are stated on the label and in each product's data sheet.
Which certifications do you hold?
U.Jet operates a quality system certified to ISO 9001 and ISO 13485. The devices are CE-marked under Regulation (EU) 2017/745 (MDR).
What is the EN 13795 standard?
It is the European standard defining the barrier requirements (resistance to liquids and microorganisms) of surgical drapes and gowns, with two levels: Standard Performance and High Performance. Each product's level is stated in its technical data sheet.
Where do you manufacture?
In-house in Italy, with a controlled production cycle from raw material to sterilization, since 1983.
Can I request customized products?
Yes. We make drapes, gowns and procedure packs tailored to the customer's needs. Contact us for an assessment.
How do I request a quote or documentation?
From each product page you can send a pre-filled quotation request, or write to info@ujet.it. Data sheets and declarations of conformity are available on request.
What is the packaging and shelf life?
The number of pieces per carton and the shelf life are stated on each product's page.