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Stirixis Αυτοκολλητη Γαζα Αποστειρωμενη 10Χ10CM 50ΤΜΧ

by Λαμεντ Ικε EUDAMED

Active European Union

Ref 5213012320010Model STIRIXIS ΕΠΙΔΕΣΜΟΣ ΕΛΑΣΤΙΚΟΣ 5cm X 4,5m

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number521301232AnalosimaLG Basic UDI-DIDate18 May 2022RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • 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
STIRIXIS ΕΠΙΔΕΣΜΟΣ ΕΛΑΣΤΙΚΟΣ 5cm X 4,5m
Model / Reference
STIRIXIS ΕΠΙΔΕΣΜΟΣ ΕΛΑΣΤΙΚΟΣ 5cm X 4, 5m, 5213012320010
Primary DI / UDI-DI
05213012320010
Basic UDI-DI
521301232AnalosimaLG
Direct Marketing DI
05213012320010
EMDN Code
M04010101 Non-woven adhesive dressings, with absorbent pad
Device Class
Class I
Market of Registration
Greece

Manufacturer details

EUDAMED SRN
GR-MF-000020993

Other devices from Λαμεντ Ικε

See all devices from Λαμεντ Ικε →

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