Shenzhen Aeon Technology Co., Ltd.

Certificate G15 073767 0021

Rev. Rev. 00Supplemented

Valid until: Apr 4, 2029

Certificate G15 073767 0021 is a valid Quality management system issued to Shenzhen Aeon Technology Co., Ltd. and registered in EUDAMED. Valid until April 4, 2029. View the full certificate record on MD Atlas.

Overview

Certificate number: G15 073767 0021
Certificate type: Quality management system
Certificate status: Supplemented
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Version: 1
Certificate ID: 0123G15 073767 0021Rev. 00

Validity

Issued: Jun 22, 2026
Valid from: Jun 22, 2026
Valid until: Apr 4, 2029

Manufacturer

Manufacturer: Shenzhen Aeon Technology Co., Ltd.
Manufacturer SRN: CN-MF-000012690
Manufacturer country: China

Notified body

Notified body
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

History

Status changes

Supplemented

Supersedes

G10 073767 0018AmendedJul 4, 2025 → Apr 4, 2029

Predecessor certificate not registered in EUDAMED.

Scope coverage

Class IIa3

3 scopes

MDA 0203 - Active non-implantable devices for monitoring of vital physiological parameters
Class IIa
MDA 0307 - Active non-implantable respiratory devices
Class IIa
MDN 1201 - Non-active non-implantable devices for anaesthesia, emergency and intensive care
Class IIa

Documents

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