← Back to catalogue

NervecentreEPR

EUDAMED

Class I (EU MDR)

Ref NervecentreEPR

by Nervecentre Software Ltd

Identity

Trade Name
NervecentreEPR EUDAMED
Device Name
NervecentreEPR EUDAMED
Model / Reference
NervecentreEPR EUDAMED

Identifiers

Primary DI / UDI-DI
05060615290000 EUDAMED
Basic UDI-DI
506061529NervecentreEPRMR EUDAMED
EMDN Code
Z12040282 GENERAL MEDICINE THERAPEUTIC TREATMENT INSTRUMENTS - SOFTWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Special Device Type
Software EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

NervecentreEPR by Nervecentre Software Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
UK-MF-000042892
Authorised Representative
European Healthcare & Device Solutions Ltd. IE-AR-000003999

Sources (1)

  • EUDAMED 1ab83471-96be-4924-be9c-0271f126c8b5 61 fields · synced Oct 6, 2026