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PHYSIODOSE sérum physiologique stérile

by Laboratoires Gilbert EUDAMED

Active European Union

Ref 626663, 626739, 626663V1

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberB-03518646266638 Basic UDI-DIDate17 Apr 2023RegisteredStatusActive
European UnionCE/MDD NumberB-03518646266638 Basic UDI-DIDate17 Apr 2023RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR, CE/MDD Active

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Specification

EUDAMED

Trade Name
PHYSIODOSE sérum physiologique stérile
PHYSIODOSE Sérum physiologique
Device Name
Sterile 0.9% solution of sodium chloride, in unidose container
Model / Reference
626663, 626739, 626663V1
Primary DI / UDI-DI
03518646266638, 03518646267390
Basic UDI-DI
B-03518646266638, 3518640000087H
EMDN Code
Q0299,Q030103,V9099
Device Class
Class IIa
Class IIb
Market of Registration
France
Belgium

Manufacturer details

EUDAMED SRN
FR-MF-000001710

Other devices from Laboratoires Gilbert

See all devices from Laboratoires Gilbert →

Properties

  • Sterile

Other properties (12)

  • 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