Easy to open/close. Drains ¼ US-gallon in 14 seconds, 1 litre in 15 seconds

These components are manufactured in Denmark by Injection Molding, securing high quality, low unit prices, focus on sustainability and respect for the environmental impact of production.

  • Variants on stock shipped worldwide within 5 businessdays
  • Variants on stock available in small quantities
  • Can be ordered in other colors and materials
  • Can be sterilized and maintain functionality ***
  • Produced in Denmark using quality raw materials from EU-based suppliers

Carmo A/S's quality management system is certified to ISO 13485:2016 Medical devices quality management system by Bureau Veritas (accredited by DANAK), certificate no. DK020611. Scope: Design, development, manufacture and assembly of injection molded plastic components. Valid: 2. September 2026 – 1. September 2029.

All Carmo plastic components are manufactured under the same QMS and procedures.

Order#MaterialColorFrom stockStandard PackProper-
ties
UseCommentsMOQ
(pcs.)
In stock
(pcs.)
Price
09-855-7222PVC+ABS
1 x 1.200 1.200 -

Need a smaller quantity? Tell us how many you need. We may be able to repack for a fee, or refer you to one of our distributors.

Need a price, or another color or material?
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All measurements and drawings are nominal. For exact measurements - and for critical integration - please contact sales for detailed drawings. Carmo is not responsible for misprints and technical changes.

Please note: Products in PVC are inherently susceptible to deformation due to elevated temperatures during storage and transportation. Carmo recommends storing and transporting components between 0 and 30 deg Celsius. In order to help minimise this risk, all Carmo products are shipped in extremely rigid cartons with a comparatively small number of parts per box.


(*) Smaller quantities can be delivered on request for a repacking fee.

(**) Stocklevels are indicative.

(***) Carmo's Medical components are designed to be able to withstand common sterilisation. However, it is the responsibility of the customer to verify the product's resilience to any specific sterilisation process.