Statistics for Picterus AS

3Total Devices

2Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

2Countries

Certificate health for Picterus AS

No certificates registered for this manufacturer.

Showing 1–3 of 3 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
Picterus® Calibration Card	`07073087007623`	`07073087007623`	1	On the market
Picterus® Calibration Card	`00763`	`07073087007630`	1	On the market
Picterus® Jaundice Pro	`00028`	`07073087000082`	1	On the market

Devices placed in 2 countries

EUDAMED update: Jun 26, 2024

NO-MF-000002136

Active

THOMSEN Tormod
Article 15 Person responsible for regulatory compliance (Substitute) Manufacturers shall have available within their organisation at least one person responsible for regulatory compliance who possesses the requisite expertise in the field of medical devices. The requisite expertise shall be demonstrated as outlined in Article 15 of the Medical Devices Regulation (EU) 2017/745 - MDR.
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ÅSLUND Alma
Article 15 Person responsible for regulatory compliance Manufacturers shall have available within their organisation at least one person responsible for regulatory compliance who possesses the requisite expertise in the field of medical devices. The requisite expertise shall be demonstrated as outlined in Article 15 of the Medical Devices Regulation (EU) 2017/745 - MDR.
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