Questionnaire for market observation of port catheter systems

Customer feedback Patient English

Dear Sir or Madam,

Against the background above, we are dependent on your support within the framework of the practical implementation of the EU Regulation 2017/745 enacted by the European Parliament and the Council.

Dear Sir or Madam, Against the background above, we are dependent on your support within the framework of the practical implementation of the EU Regulation 2017/745 enacted by European Parliament and the Council. The evaluation of your answers is anonymous and no conclusions about individual patients are included in the corresponding evaluation.

The questionnaire is divided into the following topics:

I. Information about the patient
II. product details
III. Treatment information
IV. Information on the implant (port catheter system)
V. General

Please take 5-10 minutes to answer the questionnaire.
Your answers will help us to improve medical products in the future, to make them even safer and to make them available in the usual form.

Thank you very much for your support!
The team of PakuMed gmbh

Contact:

PakuMed medical products gmbh

Im Löwental 79
45239 Essen

E-Mail: info@pakumed.de
Tel.: +49 201 – 43 70 97 – 0
** If you have been implanted with a port catheter system from the manufacturer PakuMed medical products gmbh (Essen, Germany), you will find information on the article no. and lot in your implantation certificate.
Satisfaction (0= dissatisfied, 4=very satisfied)