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Aiguille rétrobulbaire 25G

by Laboratoire De Contactologie Appliquee - Lca France EUDAMED

Ref R1637CModel RHEXIS Aiguille EMDN A010504

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-03700288635426 Basic UDI-DIDate5 Mar 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Aiguille rétrobulbaire 25G - Boite de 100
Model / Reference
RHEXIS Aiguille, R1637C
Primary DI / UDI-DI
03700288635426
Basic UDI-DI
B-03700288635426
EMDN Code
A010504 Retrobulbar needles
Device Class
Class IIa
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000001732

Other devices from Laboratoire De Contactologie Appliquee - Lca

See all devices from Laboratoire De Contactologie Appliquee - Lca →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Administering Medicine
Other properties (9)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED bb6e3e8f-31c4-446c-92d9-0fc69d08882d 61 fields · synced 24 Oct 2026