Zhejiang Soudon Medical Technology Co.,Ltd

Certificate M.2025.MDR.1070

Rev. 00Withdrawn

Valid until: Apr 7, 2030

Certificate M.2025.MDR.1070, a Quality management system issued to Zhejiang Soudon Medical Technology Co.,Ltd, has been withdrawn. View the full certificate record on MD Atlas.

Overview

Certificate number: M.2025.MDR.1070
Certificate type: Quality management system
Certificate status: Withdrawn
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Version: 2
Certificate ID: 2696M.2025.MDR.107000

Validity

Issued: Apr 8, 2025
Valid from: Apr 8, 2025
Valid until: Apr 7, 2030

Manufacturer

Manufacturer: Zhejiang Soudon Medical Technology Co.,Ltd
Manufacturer SRN: CN-MF-000021047
Manufacturer country: China

Notified body

Notified body
Notified body SRN: 2696
Notified body country: Croatia

Covered devices

No specific devices are listed for this certificate.

Characteristics

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

History

Status changes

Withdrawn

Supersedes

M.2025.MDR.1070Quality management systemIssuedApr 8, 2025 → Apr 7, 2030

Scope coverage

Class IIa1

1 scope

Sterile, Disposable Biopsy Forceps Sterile, Disposable Endoscope Injection Needles
Class IIa

Documents

LanguagesEN