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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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Documents

Neuromedical Sp z o.o.

Certificate HZ 2509180-1

Rev. 0Issued

Valid until: May 22, 2030

Overview

Certificate number: HZ 2509180-1
Certificate type: Quality management system
Certificate status: Issued
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Version: 1
Certificate ID: 0197HZ 2509180-10

Validity

Issued: May 23, 2025
Valid from: May 23, 2025
Valid until: May 22, 2030

Manufacturer

Manufacturer: Neuromedical Sp z o.o.
Manufacturer SRN: PL-MF-000040055
Manufacturer country: Poland

Notified body

Notified body: TÜV Rheinland LGA Products GmbH
Notified body SRN: 0197
Notified body country: Germany

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: Yes
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

No status changes or preceding certificates are recorded.

Scope coverage

Class IIa1

1 scope

N010103 – Neurophysiology devices Bipolar nervous electrostimulators, batterypowered
Class IIa

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