Statistics for NO

3Total Devices

3Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

1Countries

Certificate health for NO

No certificates registered for this manufacturer.

Devices by risk class

Device catalog for NO

Showing 1–3 of 3 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
20120070	`20120070`	`07350081780043`	7	On the market
30120070	`30120070`	`07350081780111`	7	On the market
400041601	`400041601`	`07350081780395`	1	On the market

Device families (Basic UDI-DI) of NO

Showing 1–3 of 3 device families.

Market presence of NO

Devices placed in 1 country

Sweden3

EUDAMED update: Jun 10, 2024

NoseOption AB

SE-MF-000025669

Active

Address: Surbrunnsgatan, 42 113 48 Stockholm
Role: Manufacturer
Date of registration: Jul 5, 2022
Country: SE Sweden

About NO

SRN: SE-MF-000025669
Role: Manufacturer
Country: Sweden
Organization name: NoseOption AB
EU VAT number: SE556861229401
EORI: SE5568612294
Date of registration: Jul 5, 2022

Contact details for NO

Address: 42, SURBRUNNSGATAN 113 48 STOCKHOLM SWEDEN
Email: alexis.ruin@nosaplugs.com
Website: nosaplugs.com

Validator

Name: Swedish Medical Products Agency
SRN: SE-CA-030
Phone: +46 18 17 46 00
Email: registrator@lakemedelsverket.se

Officers and regulatory representatives of NO

RUIN Alexis
The conformity of medical devices is checked in accordance with the QMS under these devices are manufactured before a product is released That the technical documentation and the declaration of conformity are drawn up and kept up to date That post-market plans are written and followed up Vigilance/MDR reporting In case of investigational devices in a clinical investigation , writing the statement that the device in question conforms to the general safety and performance requirements
Hidden

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