Impressum - verantwortlich für den Inhalt

Re5 ApS 
Niels Ebbesens Vej 31 
1911 Frederiksberg (Kopenhagen) 
Dänemark 
Phone: +45 5053 1410 
Re5.com 

Geschäftsführung:  
Peter Schøller-Larsen  

Rechtsform: ApS 
Sitz: Frederiksberg (Kopenhagen) 
Amtsgericht Kopenhagen 
Registernummer: 10039266 
 
USt-IdNr.: P 1007757448  

Inhaltlich Verantwortliche gemäß § 5 TMG (Telemediengesetz):  
Peter Schøller-Larsen 
(Anschrift wie oben) 

Disclaimer

Wir haben auf unseren Seiten Links zu Seiten im Internet gelegt, deren Inhalt und Aktualisierung nicht dem Einflussbereich der Re5 ApS unterliegen. Deshalb kann die Re5 ApS für diese Inhalte auch keine Gewähr übernehmen. Diese Erklärung gilt für alle auf unserer Homepage angezeigten Links und für alle Inhalte der Seiten, zu denen die bei uns angemeldeten Banner und Links führen. 


Copyright

Das Layout der Homepage, die verwendeten Grafiken und Bilder sowie die einzelnen Beiträge sind urheberrechtlich geschützt. Die fotomechanische Wiedergabe, die Vervielfältigung und die Verbreitung mittels besonderer Verfahren (zum Beispiel Datenverarbeitung, Datenträger und Datennetze) - auch auszugsweise - ist nur nach Genehmigung durch die Re5 ApS gestattet. 

COMPANY

Re5 ApS

Niels Ebbesens Vej 31

1911 Frederiksberg C Copenhagen, Denmark

E-mail: info@re5.com

© 2026 Re5 Regeneration. All rights reserved.

REGULATORY AND LEGAL NOTICE


Re5 ApS — Danish medical device manufacturer

CE MDR Class IIa | EU MDR 2017/745 | ISO 13485 | IEC 60601

Re5 is a registered medical device manufacturer in the EU. This website and its content are produced in accordance with EU MDR 2017/745 and applicable Danish medical device advertising regulations. For regulatory enquiries or to request clinical documentation, contact us directly.

This website is intended for healthcare professionals and institutional decision-makers. Some illustrative images are AI-generated. All clinical claims are supported by clinical data, including peer-reviewed scientific literature, as documented in the Clinical Evaluation Report prepared in accordance with EU MDR requirements.

COMPANY

Re5 ApS

Niels Ebbesens Vej 31

1911 Frederiksberg C Copenhagen, Denmark

E-mail: info@re5.com

© 2026 Re5 Regeneration. All rights reserved.

REGULATORY AND LEGAL NOTICE


Re5 ApS — Danish medical device manufacturer

CE MDR Class IIa | EU MDR 2017/745 | ISO 13485 | IEC 60601

Re5 is a registered medical device manufacturer in the EU. This website and its content are produced in accordance with EU MDR 2017/745 and applicable Danish medical device advertising regulations. For regulatory enquiries or to request clinical documentation, contact us directly.

This website is intended for healthcare professionals and institutional decision-makers. Some illustrative images are AI-generated. All clinical claims are supported by clinical data, including peer-reviewed scientific literature, as documented in the Clinical Evaluation Report prepared in accordance with EU MDR requirements.

COMPANY

Re5 ApS

Niels Ebbesens Vej 31

1911 Frederiksberg C Copenhagen, Denmark

E-mail: info@re5.com

© 2026 Re5 Regeneration. All rights reserved.

REGULATORY AND LEGAL NOTICE


Re5 ApS — Danish medical device manufacturer

CE MDR Class IIa | EU MDR 2017/745 | ISO 13485 | IEC 60601

Re5 is a registered medical device manufacturer in the EU. This website and its content are produced in accordance with EU MDR 2017/745 and applicable Danish medical device advertising regulations. For regulatory enquiries or to request clinical documentation, contact us directly.

This website is intended for healthcare professionals and institutional decision-makers. Some illustrative images are AI-generated. All clinical claims are supported by clinical data, including peer-reviewed scientific literature, as documented in the Clinical Evaluation Report prepared in accordance with EU MDR requirements.