Q-Med AB

Certificate 2268181CE02

Rev. 0Issued

Valid until: Aug 1, 2030

Certificate 2268181CE02 is a valid Quality management system issued to Q-Med AB and registered in EUDAMED. Valid until August 1, 2030. View the full certificate record on MD Atlas.

Overview

Certificate number: 2268181CE02
Certificate type: Quality management system
Certificate status: Issued
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Version: 1
Certificate ID: 03442268181CE020

Validity

Issued: Dec 3, 2025
Valid from: Dec 3, 2025
Valid until: Aug 1, 2030

Manufacturer

Manufacturer: Q-Med AB
Manufacturer SRN: SE-MF-000008549
Manufacturer country: Sweden

Notified body

Notified body
Notified body SRN: 0344
Notified body country: Netherlands

Covered devices

Characteristics

Sterile: Yes
Human tissues: No
Animal tissues: No
In vitro diagnostics: No
Initial registration: Yes
New device: No
Discard allowed: No
SSCP enabled: No
Mechanism of scrutiny: No
Intended medical purpose: Yes
SPP applicable

History

No status changes or preceding certificates are recorded.

Scope coverage

Class III2

2 scopes

DEVICE
Class III
DEVICE
Class III

Documents

LanguagesEN