Resvent Medical Technology Co., Ltd.

Certificate G15 096632 0018

Rev. Rev. 01Reissued

Valid until: Oct 23, 2029

Certificate G15 096632 0018 is a valid Quality management system issued to Resvent Medical Technology Co., Ltd. and registered in EUDAMED. Valid until October 23, 2029. View the full certificate record on MD Atlas.

Overview

Certificate number: G15 096632 0018
Certificate type: Quality management system
Certificate status: Reissued
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Version: 1
Certificate ID: 0123G15 096632 0018Rev. 01

Validity

Issued: Jun 15, 2026
Valid from: Jun 15, 2026
Valid until: Oct 23, 2029

Manufacturer

Manufacturer
Manufacturer SRN: CN-MF-000012608
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: Yes
Intended medical purpose: No
SPP applicable

History

Supersedes

G15 096632 0018IssuedApr 23, 2025 → Jun 14, 2026
G15 096632 0020IssuedOct 28, 2025 → Jun 14, 2026

Predecessor certificate not registered in EUDAMED.

Scope coverage

Class IIa2Class IIb1

3 scopes

MDA 0307 - Active non-implantable respiratory devices
Class IIa
Z120301 - ANAESTHESIA AND PULMONARY VENTILATION SUPPORT INSTRUMENTS
Class IIb
MDA 0315 - Software
Class IIa

Documents

LanguagesEN