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Terumo Syringe with Needle

by Terumo (Philippines) Corporation 38 variants

Ref SS+03L2332

Active European Union

CE MDR

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number48060175SSNY5 Basic UDI-DI 14806017500075UDI-DIDate14 Oct 2026RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Model / Reference
SS+03L2332
Primary DI / UDI-DI
14806017500075
Basic UDI-DI
48060175SSNY5
EMDN Code
A020102020101 Infusion and irrigation syringes, luer lock cone, 3-piece with needle, single-use
Device Class
Class IIa
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
PH-MF-000001794
Authorised representative
TERUMO EUROPE N.V. BE-AR-000001433

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Properties

  • Sterile
  • CMR Substance
  • Administering Medicine
  • Measuring Function

Other properties (9)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Incorporates Medicinal Product: No