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Baby Nadif Isotonic

by Crab Sinergy Srl EUDAMED

Active European Union

Ref BNIS001

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number803377670192350MA Basic UDI-DIDate6 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • EPT 0477.MDR.25/6034 Issued

    Quality management system EU MDR

    Notified body
    Notified body 0477
    Issued
    22 Dec 2025
    Expires
    14 May 2030

Specification

EUDAMED

Device Name
Nadif Sea Water Family
Model / Reference
BNIS001
Primary DI / UDI-DI
08033776700951
Basic UDI-DI
803377670192350MA
Direct Marketing DI
08033776700951
EMDN Code
Q030199 Nasopharyngeal devices - other
Device Class
Class IIa
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000008825

Other devices from Crab Sinergy Srl

See all devices from Crab Sinergy Srl →

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