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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Qliora AB — Manufacturer in Sweden

MD Atlas update: May 27, 2026

Qliora AB

SE-MF-000052762

Active

Address: Edvard Griegsgången, 13 16432 Kista, Stockholm
Role: Manufacturer
Date of registration: Mar 18, 2026
Country: SE Sweden

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About Qliora

SRN: SE-MF-000052762
Role: Manufacturer
Country: Sweden
Organization name: Qliora AB
EU VAT number: SE559547468401
Trade register: 559547-4684
Date of registration: Mar 18, 2026

Contact details for Qliora

Address: 13, EDVARD GRIEGSGÅNGEN 16432 KISTA, STOCKHOLM SWEDEN
Phone: +46735780807
Email: legal@qliora.com
Website: qliora.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 Qliora

MAJID Srmed
Ensuring Liora Vox maintains compliance with EU MDR 2017/745 Class I requirements including: quality management system maintenance, technical documentation accuracy, post-market surveillance, vigilance reporting, device safety and performance monitoring, and ensuring the device operates within its intended purpose as a clinical documentation tool with human oversight of all output.
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Device catalog for Qliora

Showing 1–1 of 1 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
LV-001	`LV-001`	`07300009084876`	1	On the market

Certificate health for Qliora

No certificates registered for this manufacturer.

Statistics for Qliora

1Total Devices

1Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

1Countries

Market presence of Qliora

Devices placed in 1 country

Sweden1

Devices by risk class