Statistics for Lilleborg

9Total Devices

6Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

1Countries

Certificate health for Lilleborg

No certificates registered for this manufacturer.

Devices by risk class

Device catalog for Lilleborg

Showing 1–9 of 9 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
3575	`3575`	`07046110210369`	1	On the market
3481	`3481`	`07046110207765`	1	On the market
9308264	`9308264`	`07615400234943`	1	On the market
7584	`7584`	`07046110197202`	1	On the market
3774	`3774`	`07046110218426`	1	On the market
3423	`3423`	`07046110206249`	1	On the market
3832	`3832`	`07046110220528`	1	On the market
3737	`3737`	`07046110217580`	1	On the market
3623	`3623`	`07046110213193`	1	On the market

Device families (Basic UDI-DI) of Lilleborg

Showing 1–6 of 6 device families.

Market presence of Lilleborg

Devices placed in 1 country

Norway9

EUDAMED update: Jan 6, 2026

Lilleborg AS

NO-MF-000012956

Active

Address: Hoffsveien , 21/23 0214 Oslo
Role: Manufacturer
Date of registration: Sep 9, 2021
Country: NO Norway

About Lilleborg

SRN: NO-MF-000012956
Role: Manufacturer
Country: Norway
Organization name: Lilleborg AS
EU VAT number: NO 925745855 MVA
Trade register: NO 925745855
Date of registration: Sep 9, 2021

Contact details for Lilleborg

Address: 21/23, HOFFSVEIEN 0275 OSLO 0214 OSLO NORWAY
Phone: +4781536000
Email: kundeservice.lilleborg@solenis.com
Website: https://www.lilleborg.no/

Validator

Name: The Norwegian Medical Products Agency
SRN: NO-CA-032
Phone: +47 22 89 77 00
Email: Meddev-no@noma.no

Officers and regulatory representatives of Lilleborg

RØRMARK Lisbeth
Essential Duties and Responsibilities: Among additional duties, the main responsibilities are the one mentioned in Article 15 of the EU MDR 2017/745: 1. Conformity of the product device to the Medical Device Regulation and Quality Management System 2. Conformity of the Technical Documentation and EU Declaration of conformity 3. Compliance with Post-Market Surveillance (PMS) following Article 10(10) 4. Compliance with the Vigilance Reporting obligations (Article 87 to 91)
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