CuraMedical can rely on a substantial record of sales without reportable complaints or adverse incidents which has proven our product’s efficacy and performance. The quality manual of CuraMedical B.V. and further required documented procedures have been reviewed by the notified body MDC (CE 0483) with respect of the requirements of the Medical Device Directive 93/42/EEC, Annex II, and EN ISO 13485:2016.
Download our ISO 13485:2016 Quality Management System Certificate

The design dossiers and technical files for the products Curaspon®, Curacel® and Curatamp® have been successfully examined and awarded CE certification by Notified Body MDC, Stuttgart, Germany (CE0483). Our EC certificates and Declarations of Conformity (DOC) can be downloaded below:

CuraMedical EC Quality System Certificate for the full scope of Sterile absorbable and non-absorbable haemostats
CuraSpon EC Design Examination Certificate and CuraSpon DOC
CuraCel Standard EC Design Examination Certificate and CuraCel Standard DOC
CuraCel High Density EC Design Examination Certificate and CuraCel High Density DOC
CuraCel Fibrillar EC Design Examination Certificate and CuraCel Fibrillar DOC
CuraTamp Standard EC Design Examination Certificate and CuraTamp Standard DOC
CuraWax EC Design Examination Certificate and CuraWax DOC

Instructions for use

CuraCel Standard, Fibrillar, High Density
CuraTamp
CuraSpon
CuraWax

CuraMedical - Brochure

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