FLUIDDA NV

Certificate 20M00107CRT01

Cancelled

Valid until: Jun 21, 2025

Certificate 20M00107CRT01, a Quality management system issued to FLUIDDA NV, has been withdrawn. View the full certificate record on MD Atlas.

Overview

Certificate number: 20M00107CRT01
Certificate type: Quality management system
Certificate status: Cancelled
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Version: 2
Certificate ID: 191220M00107CRT01

Validity

Issued: Jun 21, 2022
Valid from: Jun 21, 2022
Valid until: Jun 21, 2025

Notified body

Notified body: Kiwa Assurance B.V.
Notified body SRN: 1912
Notified body country: Netherlands

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: No
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

Status changes

Cancelled

Supersedes

20M00107CRT01Quality management systemIssuedJun 21, 2022 → Jun 21, 2025

Scope coverage

Class IIa2

2 scopes

MDA 0315
Class IIa
Broncholab
Class IIa

Documents

LanguagesEN