What is supplied?
The MUMD single-use balloon catheter inflation device (20 ml, 30 atm, class I, sterile, mechanical gauge) and the hospital recycling guide. See the product page.
How is a quote prepared?
You send your hospital name and rough yearly device volume through the quote form. We review the request and contact you directly to agree the quotation. You can estimate your effect first with the calculator.
What documents are available?
The recycling guide comes with the quote. The study behind the environmental numbers and the claim register are public on the evidence page. Other technical and regulatory documents are available on request. Tell us what your hospital needs in the quote form.
What is the minimum order quantity?
1,000 units. If your need is lower, contact us directly and we will look at options.
Why procurement teams ask for it
Lower spend
12.5% guaranteed reduction on your current annual spend, confirmed in your quote.
Less waste
About 84% of each device by mass goes to recycling instead of incineration.
Lower CO₂e
Around 225 g CO₂e less end-of-life emissions per device in the study model.
Ordering details
Ordering process
- Send hospital name, yearly volume and delivery country via the quote form.
- We reply with a quotation and the recycling guide.
- After you accept, we confirm quantity, delivery address and schedule in writing.
Minimum order: 1,000 units.
Lead time and geography
- First order
- About 3 months
- Repeat orders
- 3-4 weeks from stock
- Delivery countries
- Confirmed per quote
Packaging
Devices are supplied sterile, single-use. Packaging format and units per carton are confirmed in the quotation.
Recycling responsibilities
MUMD does not collect or recycle used devices for the hospital. The hospital handles recycling itself, using its own waste or recycling contractor.
The recycling guide supplied with the quote describes how to collect the used devices and remove the pressure gauge.
Document requests
Name the documents you need (for example technical file extracts, declarations, safety data) in the quote form or by email to naveen@mumd.ch. The quote reply confirms which documents exist and when they can be shared. Documents not yet available are listed as such.
Regulatory status
CE marked, certified by an EU notified body (class I, sterile). The certificate and declaration of conformity are not published on this site. Request them with your quote for tender files.
Ready to talk? Send hospital name and rough yearly device volume. We reply with a quote and the recycling guide.