EU Medical Device Regulation (MDR) 2017/745

Picterus AS is the legal manufacturer of a class IIa medical device, the Picterus® Jaundice Pro, and a class I medical device, the Picterus Calibration Card. Picterus AS is certified under the European Medical Device Regulation 2017/745 and holds the following certificates:

ISO 13485

2017/745 MDR certificate

Instructions for use

EU including EEA region

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Non EU region

Language Version

Card Holder

Historic Instructions for use

Note that these Instructions for Use are provided for reference, but are no longer up to date.

Language Version

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Access our neonatal jaundice and Picterus Jaundice Pro e-learning course

This Course will equip you with the essential knowledge and practical skills to confidently assess and manage neonatal jaundice, using tools like Picterus® Jaundice Pro for accurate screening. You’ll also explore clinical guidelines and best practices to ensure that your decisions align with clinical recommendations.

The course is free! Sign up today!

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