Protektor32 Pods and Pod Kit

by Natus Medical Incorporated Dba Excel-Tech Ltd (Xltek) 8 variants

Ref 002934

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number038283NA00095EQ Basic UDI-DI 00382830060141UDI-DI	Date15 Jan 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: P32 ACQ Pod combine kit
Model / Reference: 002934

Primary DI / UDI-DI: 00382830060141
Basic UDI-DI: 038283NA00095EQ
Direct Marketing DI: 00382830060141
EMDN Code: Z129013 General auditory and/or visual stimulators

Device Class: Class I
EU market of registration: Ireland

Manufacturer details

EUDAMED SRN: CA-MF-000004001
Authorised representative: Natus Manufacturing Ltd IE-AR-000000884

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Properties

Other properties (13)

Sterile: No
Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No