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Surflo-S Plus Straight I.V. Catheter

by Delta Med SPA 9 variants

Ref SR+DM1832SDModel Standard Peripheral IV Catheters

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8032248200006Z Basic UDI-DI 08032248200845UDI-DIDate7 Jul 2023RegisteredStatusActive

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  • Withdrawn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
Standard Peripheral IV Catheters, SR+DM1832SD
Primary DI / UDI-DI
08032248200845
Basic UDI-DI
8032248200006Z
Direct Marketing DI
08032248200845
EMDN Code
C0101010102 Peripheral i.v. catheters, w/o safety systems, w/o injection valves
Device Class
Class IIa
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
IT-MF-000027962

Other devices from Delta Med SpA

See all devices from Delta Med SpA →

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