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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

NEURANIX S.R.L.

Certificate ITH 2429564 1

Rev. 01Supplemented

Valid until: May 17, 2028

Overview

Certificate number: ITH 2429564 1
Certificate type: Quality management system
Certificate status: Supplemented
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Version: 2
Certificate ID: 1936ITH 2429564 101

Validity

Issued: May 18, 2023
Valid from: May 18, 2023
Valid until: May 17, 2028

Manufacturer

Manufacturer: NEURANIX S.R.L.
Manufacturer SRN: IT-MF-000034344
Manufacturer country: Italy

Notified body

Notified body: TUV Rheinland Italia SRL
Notified body SRN: 1936
Notified body country: Italy

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

Supplemented

Supersedes

ITH 2429564 1Quality management systemIssuedMay 18, 2023 → May 17, 2028

Scope coverage

Class IIa1

1 scope

Dispositivi non impiantabili attivi per otorinolaringoiatria / Active non-implantable devices for ear, nose and throat
Class IIa

Documents

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