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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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MD Atlas
Documents

ANACONDA BIOMED, S.L.

Certificate 2266433CE01

Rev. Rev. 0Issued

Valid until: Jun 1, 2030

Overview

Certificate number: 2266433CE01
Certificate type: Quality management system
Certificate status: Issued
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Version: 1
Certificate ID: 03442266433CE01Rev. 0

Validity

Issued: Jun 4, 2025
Valid from: Jun 4, 2025
Valid until: Jun 1, 2030

Manufacturer

Manufacturer: ANACONDA BIOMED, S.L.
Manufacturer SRN: ES-MF-000009187
Manufacturer country: Spain

Notified body

Notified body: DEKRA Certification B.V.
Notified body SRN: 0344
Notified body country: Netherlands

Covered devices

ANA5 Advanced Neurovascular AccessClass III
8437019519ANAB6

Characteristics

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

History

No status changes or preceding certificates are recorded.

Scope coverage

Class III1

1 scope

DEVICE
Class III

Documents

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