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Surshield Surflash PS

by Terumo Corporation 8 variants

Ref SR*SFF2225

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 Number498735037SSRIIUD Basic UDI-DI 34987350707209UDI-DIDate7 Sep 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  • Withdrawn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

Device Name
Surshield Surflo II / Surshield Surflash PS
Model / Reference
SR*SFF2225
Primary DI / UDI-DI
34987350707209
Basic UDI-DI
498735037SSRIIUD
Unit of Use DI
04987350707208
EMDN Code
C0101010202 Peripheral i.v. catheters, with safety systems, w/o injection valves
Device Class
Class IIa
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
JP-MF-000017478
Authorised representative
TERUMO EUROPE N.V. BE-AR-000001433

Other devices from Terumo Corp.

See all devices from Terumo Corp. →

Properties

  • Sterile
  • CMR Substance
  • Administering Medicine

Other properties (10)

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