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Protektor32 Pods and Pod Kit

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

Active European Union

Ref 017900

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number038283NA00095EQ Basic UDI-DIDate15 Jan 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Device Name
P32 ACQ Pod combine kit
Model / Reference
017900
Primary DI / UDI-DI
00382830047296
Basic UDI-DI
038283NA00095EQ
Direct Marketing DI
00382830047296
EMDN Code
Z129013 General auditory and/or visual stimulators
Device Class
Class I
Market of Registration
Ireland

Manufacturer details

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

Related devices

Category: Auditory stimulator

Other devices from Natus Medical Incorporated Dba Excel-Tech Ltd (Xltek)

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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