OUR PRODUCTS

TransCutan’s operations complies with the international quality standard for medical devices ISO 13485. The quality system and the T-Port® is certified by Intertek Co. Ltd in the UK.

BUSINESS IDEA

TransCutan develops and markets the next generation access technology solution.

T-Port© system

TransCutan AB was established in 2001 with the aim to exploit unique ideas on intra-corporeal access systems, so called Transcutaneous Port systems, for short “T-Port© systems”.

CE-marking

The first T-port© was inserted in 2003 on a patient with Parkinson’s disease. Thereafter a long development period followed as a small start-up company leading eventually to certification of registration, a CE-mark in March 2014.

Hammarplast AB

To secure future financing TransCutan entered an agreement in 2012 with Hammarplast AB, a Swedish company with a business presence in medical devices.
Website

Vision

We want to become a worldwide renown and well recognized company in the field of intracorporeal access with the ambition to help patients live a better and freer life with the aid of our products

MANAGEMENT TEAM

JOHAN RYDÉN
CEO

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ELISABET REIMER-ERIKSSON
PRODUCT MANAGER

Registered nurse with long experience with different variations of dialysis treatment and renal replacement therapy, this from both public and private companies. 

As the product manager at TransCutan I am responsible for our dialysis products.

JON STARBORG
PRODUCT MANAGER

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SARAH WESTIN
MANAGER LOGISTICS AND ADMINISTRATION

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HÅKAN RANDAHL
QUALITY AND REGULATORY

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RICKARD NYMAN
MEDICAL CONSULTANT

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BOARD OF DIRECTORS

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OLA MAGNUSSON

CHAIRMAN

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DAVID BERGENDAHL

BOARD MEMBER

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RICKARD NYMAN

BOARD MEMBER

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CONTACT US

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Telephone: 08-120 572 50

Fax: 08-120 572 40

General Inquiries: info@transcutan.com

Orders: order@transcutan.com


TransCutan AB

Forskargatan 20J

SE-151 36 Södertälje

Sweden