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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

AORTICLAB s.r.l.

Certificate G12 110786 0003

Rev. Rev. 00Issued

Valid until: Feb 7, 2029

Overview

Certificate number: G12 110786 0003
Certificate type: Quality management system
Certificate status: Issued
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Version: 1
Certificate ID: 0123G12 110786 0003Rev. 00

Validity

Issued: Feb 8, 2024
Valid from: Feb 8, 2024
Valid until: Feb 7, 2029

Manufacturer

Manufacturer: AORTICLAB s.r.l.
Manufacturer SRN: IT-MF-000026729
Manufacturer country: Italy

Notified body

Notified body: TÜV SÜD Product Service GmbH
Notified body SRN: 0123
Notified body country: Germany

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: 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: Others

History

No status changes or preceding certificates are recorded.

Scope coverage

Class III1

1 scope

C01050299 - INTRAVASCULAR EMBOLIC PROTECTION CATHETERS AND SYSTEMS - OTHER
Class III

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