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RebiSmart

by Ares Trading SA Switzerland EUDAMED

Ref U6711151

EMDN A99

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4054839RebiSmart20LB Basic UDI-DIDate10 Nov 2022RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Device Name
RebiSmart 2.0
Model / Reference
U6711151
Primary DI / UDI-DI
04065266690705
Basic UDI-DI
4054839RebiSmart20LB
Direct Marketing DI
04054839397400
EMDN Code
A99 Devices for administration, withdrawal and collection - other
Device Class
Class IIa
Market of Registration
Czechia

Manufacturer details

EUDAMED SRN
CH-MF-000021799
Authorised representative
Merck Healthcare KGaA DE-AR-000007181

Other devices from Ares Trading SA

See all devices from Ares Trading SA →

Properties & raw data

Show properties, registry sources and raw records
  • Administering Medicine
  • Measuring Function
Other properties (11)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 126c2490-d744-4a26-b0fb-016568998aa0 61 fields · synced 23 Oct 2026