Skip to content

PNS DIVER Assay

by ravo Diagnostika GmbH 4 variants

Ref PNS11DIV-24Model ravo PNS11 DIVER

Active European Union

CE IVDD

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-04260737170179 Basic UDI-DI 04260737170179UDI-DIDate2 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDD Active

Specification

EUDAMED

Device Name
PNS DIVER Assay
Model / Reference
ravo PNS11 DIVER, PNS11DIV-24
Primary DI / UDI-DI
04260737170179
Basic UDI-DI
B-04260737170179
EMDN Code
W0102100299 Neuro-auto-immune disease - other
Device Class
Class IVD General
EU market of registration
France

Manufacturer details

EUDAMED SRN
DE-MF-000024780

Other devices from ravo Diagnostika GmbH

See all devices from ravo Diagnostika GmbH →

Properties

  • Professional Testing

Other properties (9)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No