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Documents

EKINNOX

Certificate G10 105291 0002

Rev. Rev. 02Issued

Valid until: Jun 21, 2026

Certificate G10 105291 0002, a Quality management system issued to EKINNOX, has expired. View the full certificate record on MD Atlas.

Overview

Certificate number: G10 105291 0002
Certificate type: Quality management system
Certificate status: Issued
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Version: 1
Certificate ID: 0123G10 105291 0002Rev. 02

Validity

Issued: Feb 20, 2025
Valid from: Feb 20, 2025
Valid until: Jun 21, 2026

Notified body

Notified body: TÜV SÜD Product Service GmbH
Notified body SRN: 0123
Notified body country: Germany

Covered devices

No specific devices are listed for this certificate.

Characteristics

Sterile: No
Human tissues: No
Animal tissues: No
In vitro diagnostics: No
Initial registration: Yes
New device: No
Discard allowed: No
SSCP enabled: Yes
Mechanism of scrutiny: No
Intended medical purpose: No
SPP applicable: No
Conditions applicable: No
MOS outside EUDAMED: —
QMS/MOS type: Others

History

No status changes or preceding certificates are recorded.

Scope coverage

Class IIa1

1 scope

Z12062582 - KINEMATIC MOTION CAPTURE ANALYSIS SYSTEMS - SOFTWARE ACCESSORIES
Class IIa

Documents

LanguagesEN

Manufacturer

Manufacturer: EKINNOX
Manufacturer SRN: FR-MF-000000917
Manufacturer country: France