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Risus

by Ri̇sus Sağlik Ürünleri̇ Sanayi̇ Ve Ti̇caret A.Ş. 17 variants

Ref SS.ST.02.NE.2325Model LUER KAYDIRMA

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08683181959996 Basic UDI-DI 08683181959996UDI-DIDate3 Dec 2025RegisteredStatusActive

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.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
2 ml Steril Hipodermik İğneli Şırınga 23Gx1"(0,60x25 mm)
Model / Reference
LUER KAYDIRMA, SS.ST.02.NE.2325
Primary DI / UDI-DI
08683181959996
Basic UDI-DI
B-08683181959996
EMDN Code
A02010499 Syringes for injector, single-use - other
Device Class
Class IIa
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000020763

Other devices from Ri̇sus Sağlik Ürünleri̇ Sanayi̇ Ve Ti̇caret A.Ş.

See all devices from Ri̇sus Sağlik Ürünleri̇ Sanayi̇ Ve Ti̇caret A.Ş. →

Properties

  • 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